Date Added to Catalog (since 11/25/08)	PubMedID	First Author	Date	Journal	Link	Study	Disease/Trait	Initial Sample Size	Replication Sample Size	Region	Reported Gene(s)	Strongest SNP-Risk Allele	SNPs	Risk Allele Frequency	p-Value	p-Value (text)	OR or beta	95% CI (text)	Platform [SNPs passing QC]	CNV
11/20/2009	19875614	Paterson	29-Oct-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19875614?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	"A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both HbA1c and glucose"	Type 1 diabetes	"1,304 diabetics"	"531 diabetics, up to 37,436 non-diabetics"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix and Illumina [2,518,578] (imputed)"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	3q28	NR	rs1152846-G	rs1152846	0.77	0.000003	(females +males)	0.09	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	19q13.3	NR	rs1878047-G	rs1878047	0.37	0.000005	(females + males)	0.06	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	19p13.3	NR	rs3803915-C	rs3803915	0.89	0.000005	(females + males)	0.13	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	11q14.1	NR	rs1458095-G	rs1458095	0.9	0.000007	(females)	0.19	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	2q36.1	NR	rs824931-G	rs824931	0.35	0.000003	(females + males)	0.07	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	4q34.3	NR	rs2383393-G	rs2383393	0.63	0.000002	(males)	0.1	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	1p36.33	NR	rs3934834-G	rs3934834	0.8	6.00E-07	(females + males)	0.11	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	3p14.1	NR	rs1024889-G	rs1024889	0.28	0.000006	(males)	0.12	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	5q35.3	NR	rs12517906-G	rs12517906	0.85	0.000006	(females)	0.16	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Body mass index	"Up to 3,925 European individuals"	NR	9p22.3	NR	rs1927702-G	rs1927702	0.42	0.000006	(females)	0.08	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	18q11.2	NR	rs1840440-G	rs1840440	0.61	3.00E-07	(females)	2.16	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	17q24.1	NR	rs7209395-G	rs7209395	0.23	0.000003	(females + males)	1.75	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	13q12.12	NR	rs2765086-G	rs2765086	0.94	0.000006	(females)	3.86	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	12p11.21	NR	rs10844154-C	rs10844154	0.54	0.000004	(females)	1.87	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	10q22.2	NR	rs7919006-G	rs7919006	0.95	0.000004	(females)	4	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	10q22.1	NR	rs1816002-G	rs1816002	0.46	0.000008	(females)	2.08	[NR] kg increase	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	3q28	NR	rs1152846-G	rs1152846	0.77	0.000006	(females + males)	1.7	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	5q35.3	MGAT1	rs12517906-G	rs12517906	0.85	7.00E-08	(females)	2.96	[NR] kg decrease	"Illumina [318,237]"	N
11/18/2009	19851299	Johansson	22-Oct-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4	Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene	Weight	"Up to 3,925 European individuals"	NR	9p13.3	NR	rs10972341-G	rs10972341	0.6	0.000009	(males)	2.32	[NR] kg increase	"Illumina [318,237]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	21q21.3	EIF4A1P	rs2830840-?	rs2830840	0.46	0.000005	(remission)	1.47	[1.23-1.72]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	18q12.1	NOL4	rs7239368-?	rs7239368	0.42	0.000009	(remission)	1.45	[1.22-1.69]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	7q36.3	UBE3C	rs6966038-?	rs6966038	0.19	5.00E-07	(response)	1.64	[1.35-1.99]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	7q36.3	UBE3C	rs6966038-?	rs6966038	0.2	4.00E-07	(remission)	1.68	[1.37-2.04]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	15q22.2	RORA	rs809736-?	rs809736	0.17	0.000008	(response)	1.52	[1.27-1.83]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	20q13.31	BMP7	rs6127921-?	rs6127921	0.82	0.000003	(response)	1.64	[1.33-2.04]	"Affymetrix [430,198]"	N
11/25/2009	19846067	Garriock	19-Oct-09	Biol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	A Genomewide Association Study of Citalopram Response in Major Depressive Disorder	Treatment response to citalopram	"Up to 883 responders, 608 non-responders"	NR	20q13.31	BMP7	rs6127921-?	rs6127921	0.81	0.000001	(remission)	1.75	[1.39-2.17]	"Affymetrix [430,198]"	N
11/12/2009	19850125	Kim	19-Oct-09	Neurobiol Dis	http://www.ncbi.nlm.nih.gov/pubmed/19850125?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Common CYP7A1 Promoter Polymorphism Associated With Risk of Neuromyelitis Optica	Neuromyelitis optica	"53 Korean cases, 240 Korean controls"	40 Korean cases	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [288,025]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	16p11.2	NR	rs7186852-A	rs7186852	0.08	3.00E-07		1.29	[1.17-1.42]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	6p21.32	HLA-DRB1	rs9271100-?	rs9271100	NR	1.00E-12		1.9	[1.59-2.27]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	2p22.3	RASGRP3	rs13385731-A	rs13385731	0.85	1.00E-15		1.43	[1.32-1.56]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	2q32.3	STAT4	rs7574865-A	rs7574865	0.33	5.00E-42		1.51	[1.43-1.61]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	5q33.1	TNIP1	rs10036748-A	rs10036748	0.76	2.00E-09		1.23	[1.15-1.33]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	6q21	"PRDM1, ATG5"	rs548234-G	rs548234	0.26	5.00E-12		1.25	[1.17-1.33]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	6q23.3	TNFAIP3	rs2230926-C	rs2230926	0.04	1.00E-17		1.72	[1.52-1.94]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	7p12.2	IKZF1	rs4917014-A	rs4917014	0.68	3.00E-23		1.39	[1.30-1.47]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	7q11.23	NR	rs1167796-G	rs1167796	0.71	2.00E-08		1.2	[1.12-1.28]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	7q32.1	IRF5	rs4728142-A	rs4728142	0.13	8.00E-19		1.43	[1.32-1.54]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	8p23.1	BLK	rs7812879-G	rs7812879	0.76	2.00E-24		1.45	[1.35-1.56]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	10q11.22	"LRRC18, WDFY4"	rs1913517-A	rs1913517	0.29	7.00E-12		1.24	[1.17-1.32]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	11q23.3	NR	rs4639966-G	rs4639966	0.3	1.00E-16		1.29	[1.22-1.37]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	11q24.3	ETS1	rs6590330-A	rs6590330	0.34	2.00E-25		1.37	[1.29-1.45)	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	12q24.32	SLC15A4	rs1385374-A	rs1385374	0.2	2.00E-11		1.26	[1.18-1.35]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	16p11.2	NR	rs7197475-A	rs7197475	0.08	3.00E-08		1.31	[1.20-1.46]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	22q11.21	"HIC2, UBE2L3"	rs131654-A	rs131654	0.48	1.00E-16		1.28	[1.20-1.35]	"Illumina [493,955]"	N
11/9/2009	19838193	Han	18-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2	Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus	Systemic lupus erythematosus	"1,047 Chinese Han cases, 1,205 Chinese Han controls"	"3,152 Chinese Han cases, 7,050 Chinese Han controls"	1q25.1	TNFSF4	rs2205960-A	rs2205960	0.27	3.00E-32		1.46	[1.37-1.56]	"Illumina [493,955]"	N
11/9/2009	19836008	Landi	15-Oct-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma	Lung adenocarcinoma	"5,739 European descent cases, 5,848 European descent controls"	"7,561 European descent cases, 13,818 European descent controls"	6p21.33	"BAT3, APOM"	rs3117582-C	rs3117582	0.1	5.00E-12		1.22	[1.15-1.29]	"Illumina [515,922]"	N
11/9/2009	19836008	Landi	15-Oct-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma	Lung adenocarcinoma	"5,739 European descent cases, 5,848 European descent controls"	"7,561 European descent cases, 13,818 European descent controls"	5p15.33	TERT	rs2736100-G	rs2736100	0.5	2.00E-10		1.12	[1.08-1.16]	"Illumina [515,922]"	N
11/9/2009	19836008	Landi	15-Oct-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma	Lung adenocarcinoma	"5,739 European descent cases, 5,848 European descent controls"	"7,561 European descent cases, 13,818 European descent controls"	6p22.1	TRNAA-UGC	rs4324798-A	rs4324798	0.09	2.00E-08		1.16	[1.09-1.24]	"Illumina [515,922]"	N
11/9/2009	19836008	Landi	15-Oct-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma	Lung adenocarcinoma	"5,739 European descent cases, 5,848 European descent controls"	"7,561 European descent cases, 13,818 European descent controls"	5p15.33	CLPTM1L	rs31489-C	rs31489	0.59	2.00E-10		1.12	[1.09-1.16]	"Illumina [515,922]"	N
11/9/2009	19836008	Landi	15-Oct-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma	Lung adenocarcinoma	"5,739 European descent cases, 5,848 European descent controls"	"7,561 European descent cases, 13,818 European descent controls"	15q25.1	"CHRNA3, CHRNA5"	rs1051730-T	rs1051730	0.35	2.00E-51		1.31	[1.27-1.36]	"Illumina [515,922]"	N
11/5/2009	19820699	Benyamin	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume	Serum markers of iron status	"4,818 Australian siblings"	"3,470 Dutch individuals"	22q12.3	TMPRSS6	rs855791-T	rs855791	0.42	1.00E-10	(MCV)	0.13	[0.09-0.17] SD decrease	"Illumina & Perlegen [427,037]"	N
11/5/2009	19820699	Benyamin	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume	Serum markers of iron status	"4,818 Australian siblings"	"3,470 Dutch individuals"	6p22.1	HFE	rs1800562-A	rs1800562	0.08	2.00E-08	(MCV)	0.22	[0.14-0.30] SD increase	"Illumina & Perlegen [427,037]"	N
11/5/2009	19820699	Benyamin	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume	Serum markers of iron status	"4,818 Australian siblings"	"3,470 Dutch individuals"	6p22.1	HFE	rs1800562-A	rs1800562	0.08	5.00E-07	(Hgb)	0.2	[0.12-0.28] SD increase	"Illumina & Perlegen [427,037]"	N
11/5/2009	19820699	Benyamin	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in TMPRSS6 are associated with iron status and erythrocyte volume	Serum markers of iron status	"4,818 Australian siblings"	"3,470 Dutch individuals"	22q12.3	TMPRSS6	rs855791-T	rs855791	0.42	5.00E-07	(Hgb)	0.1	[0.06-0.14] SD decrease	"Illumina & Perlegen [427,037]"	N
11/5/2009	19820698	Chambers	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820698?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels	Hemoglobin levels	"6,316 Europeans, 9,685 Indian Asians"	"5,187 Europeans, 6,721 Indian Asians"	6p22.1	HFE	rs198846-A	rs198846	NR	1.00E-08		NR	NR	"Affymetrix, Illumina & Perlegen [NR]"	N
11/5/2009	19820698	Chambers	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820698?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels	Hemoglobin levels	"6,316 Europeans, 9,685 Indian Asians"	"5,187 Europeans, 6,721 Indian Asians"	22q12.3	TMPRSS6	rs855791-A	rs855791	0.53	2.00E-13		0.13	[0.09-0.17] g/dl decrease	"Affymetrix, Illumina & Perlegen [NR]"	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	22q12.3	TMPRSS6	rs2413450-T	rs2413450	NR	2.00E-13		0.17	[0.13-0.22] % decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	12q24.12	"SH2B3, ATXN2"	rs11065987-G	rs11065987	NR	1.00E-12		0.17	[0.12-0.22] % decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	10q21.3	HK1	rs16926246-T	rs16926246	NR	1.00E-13		0.33	[0.24-0.42] % increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q23.3	"HBS1L, MYB"	rs9483788-C	rs9483788	NR	3.00E-15		0.22	[0.16-0.28] % increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p22.1	HFE	rs1800562-A	rs1800562	NR	2.00E-09		0.31	[0.21-0.41] % increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7q36.1	PRKAG2	rs10224002-G	rs10224002	NR	6.00E-15		0.2	[0.15-0.25] % increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7q22.1	TFR2	rs7385804-C	rs7385804	NR	4.00E-10		0.15	[0.10-0.20] % decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hematocrit	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	2p21	PRKCE	rs10168349-C	rs10168349	NR	4.00E-15		0.19	[0.14-0.23] % increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	12q24.12	TRAFD1	rs11065987-A	rs11065987	NR	1.00E-11		0.06	[0.04-0.08] g/dl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	20q13.2	TSHZ2	rs6013509-A	rs6013509	NR	1.00E-10		0.06	[0.05-0.08] g/dl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p22.1	HFE	rs1800562-A	rs1800562	NR	6.00E-19		0.16	[0.13-0.20] g/dl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	2p21	PRKCE	rs10495928-G	rs10495928	NR	7.00E-13		0.06	[0.05-0.08] g/dl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	22q12.3	TMPRSS6	rs855791-A	rs855791	NR	3.00E-25		0.09	[0.07-0.11] g/dl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	10q21.3	HK1	rs16926246-T	rs16926246	NR	2.00E-11		0.11	[0.08-0.14] g/dl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7q36.1	PRKAG2	rs10224002-G	rs10224002	NR	3.00E-15		0.07	[0.05-0.09] g/dl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	16p13.3	ITFG3	rs1122794-A	rs1122794	NR	3.00E-10		0	[0.003-0.006] pg increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	9p24.1	RCL1	rs10758658-A	rs10758658	NR	2.00E-14		0	[0.004-0.006] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p22.2	SLC17A3	rs1408272-G	rs1408272	NR	4.00E-39		0.02	[0.01-0.02] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	3q29	TFRC	rs11915082-A	rs11915082	NR	8.00E-13		0	[0.003-0.005] pg increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	19p13.13	GCDH	rs11085824-G	rs11085824	NR	1.00E-11		0	[0.003-0.005] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q24.1	CITED2	rs628751-C	rs628751	NR	1.00E-17		0	[0.003-0.005] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q23.3	"HBS1L, MYB"	rs7776054-G	rs7776054	NR	7.00E-69		0.01	[0.009-0.0111] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p21.1	"CCND3, BYSL"	rs9349205-A	rs9349205	NR	8.00E-20		0.01	[0.004-0.006] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular hemoglobin	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	22q12.3	TMPRSS6	rs2413450-T	rs2413450	NR	9.00E-34		0.01	[0.0005-0.007] pg decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	10q11.21	8-Mar	rs11239550-G	rs11239550	NR	1.00E-10		0	[0.002-0.003] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	19p13.13	RTBDN	rs7255045-A	rs7255045	NR	2.00E-12		0	[0.002-0.004] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	22q13.33	ECGF1	rs131794-A	rs131794	NR	1.00E-15		0	[0.003-0.005] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	2p16.1	BCL11A	rs2540917-C	rs2540917	NR	1.00E-14		0	[0.002-0.004] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p22.1	HFE	rs1800562-A	rs1800562	NR	1.00E-46		0.01	[0.010-0.014] fl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6p21.1	"CCND3, BYSL"	rs9349205-A	rs9349205	NR	1.00E-31		0.01	[0.004-0.006] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	14q23.3	FNTB	rs4466998-A	rs4466998	NR	5.00E-08		0	[0.001-0.003] fl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	16p13.3	ITFG3	rs7189020-T	rs7189020	NR	2.00E-12		0	[0.002-0.004] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	22q12.3	TMPRSS6	rs2413450-T	rs2413450	NR	3.00E-41		0.01	[0.004-0.006] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	3q29	TFRC	rs9859260-C	rs9859260	NR	8.00E-14		0	[0.002-0.004] fl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	4q12	KIT	rs172629-G	rs172629	NR	1.00E-15		0	[0.003-0.006] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q21	CD164	rs9374080-C	rs9374080	NR	4.00E-10		0	[0.002-0.003] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q23.3	"HBS1L, MYB"	rs4895441-G	rs4895441	NR	7.00E-86		0.01	[0.007-0.009] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q24.1	CITED2	rs643381-A	rs643381	NR	5.00E-25		0	[0.003-0.005] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7p12.2	IKZF1	rs12718597-A	rs12718597	NR	5.00E-13		0	[0.002-0.004] fl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7q22.1	TFR2	rs7786877-G	rs7786877	NR	3.00E-11		0	[0.002-0.004] fl increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Mean corpuscular volume	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	9p24.1	RCL1	rs10758658-A	rs10758658	NR	3.00E-20		0	[0.003-0.005] fl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Other erythrocyte phenotypes	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	1q23.1	SPTA1	rs857721-A	rs857721	NR	1.00E-10	(MCHC)	0	[0.001-0.002] g/dl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Other erythrocyte phenotypes	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	7q22.1	EPO	rs2075671-A	rs2075671	NR	1.00E-09	(RBC)	0	[0.005-0.009] 1 M cell/mm^3 increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Other erythrocyte phenotypes	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q23.3	"HBS1L, MYB"	rs9483788-G	rs9483788	NR	1.00E-47	(RBC)	0	[0.012-0.016] 1 M cells/mm^3 increase	Affymetrix & Illumina [~2.5 million](imputed)	N
11/3/2009	19862010	Ganesh	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium	Other erythrocyte phenotypes	"24,167 European ancestry individuals"	"9,456 European ancestry individuals"	6q23.3	"HBS1L, MYB"	rs9373124-C	rs9373124	NR	7.00E-14	(MCHC)	0	[0.002-0.003] g/dl decrease	Affymetrix & Illumina [~2.5 million](imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6q21	Intergenic	rs4947019-G	rs4947019	NR	0.000008	(MCV)	0.01	[0.003-0.011] fl decrease	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	12q24.13	PTPN11	rs11066301-G	rs11066301	NR	8.00E-12	(PLT)	4.65	[3.32-5.98] 10^9/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6p21.31	BAK1	rs210135-A	rs210135	NR	4.00E-10	(PLT)	5.44	[3.74-7.14] 10^9/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	9p24.1	AK3	rs385893-C	rs385893	NR	9.00E-17	(PLT)	6.26	[4.78-7.74] 10^9/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	17q12	"GSDMA, ORMDL3"	rs17609240-G	rs17609240	NR	9.00E-09	(WBC)	0.02	[0.01-0.03] 10^9/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6p21.32	Intergenic	rs2227139-G	rs2227139	NR	1.00E-07	(WBC)	0.02	[0.01-0.03] 10^9/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	7q22.1	TFR2	rs7385804-C	rs7385804	NR	5.00E-10	(RBC)	0.01	[0.004-0.008] 10^12/l increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6q23.3	"HBS1L, MYB"	rs9402686-A	rs9402686	NR	7.00E-42	(MCV)	0.82	[0.70-0.94] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	22q12.3	FBX07	rs9609565-G	rs9609565	NR	4.00E-10	(MCV)	0.37	[0.25-0.49] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6p21.1	"BYSL, CCND3"	rs11970772-T	rs11970772	NR	7.00E-19	(MCV)	0.58	[0.44-0.70] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	6p22.1	HFE	rs1800562-A	rs1800562	NR	1.00E-23	(MCV)	1.41	[1.13-1.69] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Hematological parameters	"4,627 European individuals"	"9,316 European individuals"	22q12.3	TMPRSS6	rs5756506-C	rs5756506	NR	1.00E-09	(MCH)	0.14	[0.10-0.18] pg increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	10q21.3	JMJD1C	rs2393967-A	rs2393967	NR	3.00E-21		0.01	[0.01-0.018] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	1q32.1	TMCC2	rs1668873-G	rs1668873	NR	1.00E-20		0.01	[0.01-0.014] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	2p23.1	EHD3	rs647316-A	rs647316	NR	3.00E-11		0.01	[0.006-0.014] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	18q22.2	CD226	rs893001-C	rs893001	NR	1.00E-10		0.01	[0.007-0.015] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	5q33.3	NR	rs1473247-C	rs1473247	NR	3.00E-07		0.01	[0.004-0.012] fl decrease	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	20p12.1	NR	rs6110278-T	rs6110278	NR	4.00E-07		0.01	[0.005-0.013] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	12q13.13	NR	rs10506328-A	rs10506328	NR	5.00E-07		0.01	[0.004-0.012] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	11p15.5	BET1L	rs11602954-G	rs11602954	NR	1.00E-14		0.01	[0.009-0.017] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	1q24.3	DNM3	rs10914144-C	rs10914144	NR	2.00E-14		0.01	[0.009-0.017] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	20p13	SIRPA	rs6136489-T	rs6136489	NR	8.00E-11		0.01	[0.006-0.014] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	15q22.2	TPM1	rs11071720-T	rs11071720	NR	2.00E-08		0.01	[0.007-0.015] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	3p14.3	ARHGEF3	rs12485738-A	rs12485738	NR	6.00E-31		0.02	[0.013-0.017] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	12q24.31	WDR66	rs7961894-T	rs7961894	NR	3.00E-44		0.03	[0.027-0.035] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	17q11.2	TAOK1	rs2138852-T	rs2138852	NR	1.00E-22		0.02	[0.012-0.020] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/30/2009	19820697	Soranzo	11-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium	Mean platelet volume	"4,627 European individuals"	"9,316 European individuals"	7q22.3	PIK3CG	rs342293-G	rs342293	NR	2.00E-33		0.02	[0.013-0.017] fl increase	Affymetrix and Illumina [~2.11 million] (imputed)	N
10/23/2009	19812673	Weiss	8-Oct-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19812673?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide linkage and association scan reveals novel loci for autism	Autism	"1,031 families with 1,553 affected offspring (multiple races/ethnicities)"	"2,073 trios (multiple races/ethnicities)"	5p15.2	"SEMA5A, TAS2R1"	rs10513025-?	rs10513025	NR	3.00E-07		1.81	[NR]	"Affymetrix [~365,000]"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	1p31.3	GPR177	rs2566755-C	rs2566755	0.21	2.00E-12		0.1	[0.07-0.13] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	8q24.12	TNFRSF11B	rs11995824-G	rs11995824	0.55	7.00E-09		0.07	[0.05-0.09] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	6q25.1	ESR1	rs2941740-G	rs2941740	0.43	2.00E-10		0.07	[0.05-0.09] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	1p36.12	ZBTB40	rs6426749-C	rs6426749	0.17	9.00E-08		0.08	[0.05-0.11] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	17q21.31	HDAC5	rs228769-G	rs228769	0.2	2.00E-08		0.08	[0.05-0.11] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	11p11.2	ARHGAP1	rs7932354-T	rs7932354	0.29	4.00E-09		0.07	[0.05-0.09] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	3p22.1	CTNNB1	rs87938-A	rs87938	0.45	8.00E-10		0.07	[0.05-0.09] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	17q21.31	CRHR1	rs9303521-T	rs9303521	0.46	0.000004		0.06	[0.04-0.07] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	16q24.1	FOXL1	rs10048146-G	rs10048146	0.19	2.00E-07		0.09	[0.06-0.12] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	11p15.2	SOX6	rs7117858-G	rs7117858	0.2	6.00E-10		0.09	[0.06-0.12] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	7q21.3	FLJ42280	rs7781370-T	rs7781370	0.34	5.00E-12		0.08	[0.06-0.10] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	5q14.3	MEF2C	rs1366594-C	rs1366594	0.45	1.00E-13		0.09	[0.07-0.11] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (hip)	"19,195 European individuals"	NR	4q22.1	MEPE	rs1471403-T	rs1471403	0.34	8.00E-07		0.06	[0.04-0.08] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	18q21.33	TNFRSF11A	rs884205-A	rs884205	0.27	9.00E-09		0.08	[0.05-0.11] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	2p16.2	SPTBN1	rs11898505-A	rs11898505	0.34	2.00E-08		0.07	[0.05-0.09] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	12q13.13	SP7	rs2016266-G	rs2016266	0.32	1.00E-08		0.07	[0.05-0.09] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	11q13.2	LRP5	rs599083-G	rs599083	0.31	5.00E-08		0.07	[0.05-0.09] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	13q14.11	AKAP11	rs9533090-T	rs9533090	0.5	5.00E-25		0.12	[0.10-0.14] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	8q24.12	TNFRSF11B	rs2062377-T	rs2062377	0.44	4.00E-16		0.09	[0.07-0.11] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	6q25.1	ESR1	rs2504063-A	rs2504063	0.4	6.00E-11		0.08	[0.06-0.10] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	1p36.12	ZBTB40	rs7524102-G	rs7524102	0.17	3.00E-10		0.09	[0.06-0.12] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	17q21.31	HDAC5	rs228769-G	rs228769	0.2	0.000004		0.07	[0.04-0.10] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	17q21.31	CRHR1	rs9303521-T	rs9303521	0.46	1.00E-08		0.07	[0.05-0.09] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	16q24.1	FOXL1	rs10048146-G	rs10048146	0.19	2.00E-08		0.09	[0.06-0.12] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	11p13	DCDC5	rs16921914-A	rs16921914	0.27	2.00E-09		0.08	[0.05-0.11] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	7q21.3	FLJ42280	rs4729260-G	rs4729260	0.32	2.00E-10		0.08	[0.05-0.11] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	4q22.1	MEPE	rs1471403-T	rs1471403	0.34	2.00E-08		0.07	[0.05-0.09] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	7p14.1	STARD3NL	rs1524058-T	rs1524058	0.4	1.00E-09		0.07	[0.05-0.09] sd decrease	"Affymetrix & Illumina [2,543,686](imputed)"	N
10/16/2009	19801982	Rivadeneira	4-Oct-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies	Bone mineral density (spine)	"19,195 European individuals"	NR	1p31.3	GPR177	rs1430742-C	rs1430742	0.21	3.00E-13		0.11	[0.07-0.14] sd increase	"Affymetrix & Illumina [2,543,686](imputed)"	N
11/4/2009	19798445	Hicks	2-Oct-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic determinants of circulating sphingolipid concentrations in European populations	Sphingolipid Concentrations	"4,110 European individuals"	NR	4p12	ATP10D	rs10938494-A	rs10938494	0.23	8.00E-19	(GluCer)	0.06	[0.04-0.07] unit increase	"Illumina [318,237]"	N
11/4/2009	19798445	Hicks	2-Oct-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic determinants of circulating sphingolipid concentrations in European populations	Sphingolipid Concentrations	"4,110 European individuals"	NR	11q12.3	FADS	rs1000778-A	rs1000778	0.32	7.00E-13	(SM 16:1)	0.62	[0.45-0.78] unit decrease	"Illumina [318,237]"	N
11/4/2009	19798445	Hicks	2-Oct-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic determinants of circulating sphingolipid concentrations in European populations	Sphingolipid Concentrations	"4,110 European individuals"	NR	14q23.2	SGPP1	rs7157785-A	rs7157785	0.19	9.00E-66	(SM 14:0Mol%)	0	[0.001-0.002] mol % increase	"Illumina [318,237]"	N
11/4/2009	19798445	Hicks	2-Oct-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic determinants of circulating sphingolipid concentrations in European populations	Sphingolipid Concentrations	"4,110 European individuals"	NR	19p13.2	LASS4	rs7258249-G	rs7258249	0.48	2.00E-27	(SM 18:1Mol%)	0	[0.0007-0.001] mol % increase	"Illumina [318,237]"	N
11/4/2009	19798445	Hicks	2-Oct-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic determinants of circulating sphingolipid concentrations in European populations	Sphingolipid Concentrations	"4,110 European individuals"	NR	20p12.1	SPTLC3	rs680379-A	rs680379	0.34	8.00E-15	(Cer24:0)	0.1	[0.08-0.13] mol % increase	"Illumina [318,237]"	N
10/6/2009	19786962	Roeske	29-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19786962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children	Speech perception in dyslexia	200 dyslexic German children	186 dyslexic German children	10q26.3	NR	rs4751178-G	rs4751178	NR	0.000007	(MMNb)	NR	NR	"Illumina [297,086]"	N
10/6/2009	19786962	Roeske	29-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19786962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children	Speech perception in dyslexia	200 dyslexic German children	186 dyslexic German children	4q32.1	"CTSO, TDO2, PDGFC"	rs4234898-T	rs4234898	NR	5.00E-08	(MMNb)	NR	NR	"Illumina [297,086]"	N
10/6/2009	19779542	Nakanishi	25-Sep-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19779542?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1	Myopia (pathological)	"297 Japanese cases, 934 Japanese controls"	"533 Japanese cases, 977 Japanese controls"	11q24.1	"BLID, LOC399959"	rs577948-G	rs577948	0.52	2.00E-07		1.37	[1.21-1.54]	"Illumina [411,777]"	N
10/5/2009	19772629	Latourelle	22-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study for Onset Age in Parkinson Disease	Parkinson disease (age of onset)	"857 white familial cases, 440 white idiopathic cases"	747 Italian idiopathic cases	2p14	AAK1	rs7577851-T	rs7577851	NR	0.000009		6.85	[NR] years younger	"Illumina and Perlegen [1,861,750] (imputed)"	N
10/5/2009	19772629	Latourelle	22-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study for Onset Age in Parkinson Disease	Parkinson disease (age of onset)	"857 white familial cases, 440 white idiopathic cases"	747 Italian idiopathic cases	11p13	"QSER1, PRRG4"	rs10767971-T	rs10767971	NR	5.00E-07		3.24	[NR] years older	"Illumina and Perlegen [1,861,750] (imputed)"	N
10/5/2009	19772629	Latourelle	22-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study for Onset Age in Parkinson Disease	Parkinson disease (age of onset)	"857 white familial cases, 440 white idiopathic cases"	747 Italian idiopathic cases	1q23.3	ATF6	rs10918270-A	rs10918270	NR	0.000008		2.26	[NR] years younger	"Illumina and Perlegen [1,861,750] (imputed)"	N
10/5/2009	19772629	Latourelle	22-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study for Onset Age in Parkinson Disease	Parkinson disease (age of onset)	"857 white familial cases, 440 white idiopathic cases"	747 Italian idiopathic cases	15q12	OCA2	rs17565841-A	rs17565841	NR	0.000003		2.84	[NR] years younger	"Illumina and Perlegen [1,861,750] (imputed)"	N
10/5/2009	19772629	Latourelle	22-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study for Onset Age in Parkinson Disease	Parkinson disease (age of onset)	"857 white familial cases, 440 white idiopathic cases"	747 Italian idiopathic cases	18q12.1	DSG3	rs1941184-C	rs1941184	NR	0.000004		2.28	[NR] years younger	"Illumina and Perlegen [1,861,750] (imputed)"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	19q13.2	Intergenic	rs8102476-C	rs8102476	0.54	2.00E-11		1.12	[1.08-1.15]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	8q24.21	Intergenic	rs445114-T	rs445114	0.64	5.00E-10		1.14	[1.10-1.19]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	3q21.3	Intergenic	rs10934853-A	rs10934853	0.28	3.00E-10		1.12	[1.08-1.16]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	8q24.21	Intergenic	rs16901979-A	rs16901979	0.04	3.00E-14		1.8	[1.55-2.09]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	8q24.21	Intergenic	rs1447295-A	rs1447295	0.11	2.00E-19		1.58	[1.43-1.74]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	8q24.21	Intergenic	rs16902094-G	rs16902094	0.15	6.00E-15		1.21	[1.15-1.26]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	11q13.2	Intergenic	rs11228565-A	rs11228565	0.2	7.00E-12		1.23	[1.16-1.31]	"Illumina [310,520]"	N
10/5/2009	19767754	Gudmundsson	20-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility	Prostate cancer	"Up to 1,968 Icelandic cases, 35,382 Icelandic controls"	"Up to 11,806 European descent cases, 12,387 European descent controls"	17q12	Intergenic	rs4430796-A	rs4430796	0.52	0.000008		1.19	[1.10-1.28]	"Illumina [310,520]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	9p22.3	NR	rs1556032-C	rs1556032	0.49	0.000009		2.05	[1.48-2.84]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	12p12.1	SOX5	rs1522232-C	rs1522232	0.52	0.000002		2.22	[1.59-3.13]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	1p13.3	Intergenic	rs4118325-G	rs4118325	0.81	6.00E-07		4.17	[2.17-8.33]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	1q23.3	RXRG	rs10800098-A	rs10800098	0.05	0.000004		3.29	[2.08-5.20]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	2q12.1	TGFBRAP1	rs1020064-G	rs1020064	0.23	0.000007		2.94	[1.75-5.00]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	8q22.3	Intergenic	rs3108919-C	rs3108919	0.27	0.000004		2.13	[1.56-2.91]	"Illumina [291,119]"	N
9/30/2009	19754311	Le Clerc	15-Sep-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03).	AIDS	"85 French cases, 2,049 French controls"	NR	9p23	Intergenic	rs1360517-A	rs1360517	0.06	0.000003		3.09	[2.00-4.78]	"Illumina [291,119]"	N
9/30/2009	19749758	Suppiah	13-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19749758?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy	Response to Hepatitis C treatment	"131 European ancestry responders, 162 European ancestry non-responders"	"261 European responders, 294 European non-responders"	19q13.2	"IL28A, IL28B"	rs8099917-G	rs8099917	NR	9.00E-09		1.98	[1.57-2.52]	"Illumina [311,159]"	N
9/30/2009	19749757	Tanaka	13-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19749757?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C	Response to Hepatitis C treatment	"72 Japanese responders, 82 Japanese non-responders"	"122 Japanese responders, 50 Japanese non-responders"	19q13.2	IL28B	rs8099917-G	rs8099917	0.12	3.00E-32		27.1	[14.6-50.3]	"Affymetrix [621,220]"	N
9/30/2009	19749422	Heinzen	11-Sep-09	J Alzheimers Dis	http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease	Alzheimer's Disease	"331 cases, 368 controls"	NR	6q24.3	SASH1	rs9390537-?	rs9390537	0.22	0.000008		NR	NR	"Illumima [~550,000]"	N
9/30/2009	19749422	Heinzen	11-Sep-09	J Alzheimers Dis	http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease	Alzheimer's Disease	"331 cases, 368 controls"	NR	13q13.2	RFC3	rs690705-?	rs690705	0.25	6.00E-07		NR	NR	"Illumima [~550,000]"	N
9/30/2009	19749422	Heinzen	11-Sep-09	J Alzheimers Dis	http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease	Alzheimer's Disease	"331 cases, 368 controls"	NR	19q13.32	"TOMM40, APOE"	rs2075650-?	rs2075650	0.15	3.00E-11		NR	NR	"Illumima [~550,000]"	N
9/30/2009	19749422	Heinzen	11-Sep-09	J Alzheimers Dis	http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease	Alzheimer's Disease	"331 cases, 368 controls"	NR	10q24.31	PAX2	rs4509693-?	rs4509693	0.18	0.000006		NR	NR	"Illumima [~550,000]"	N
9/30/2009	19749422	Heinzen	11-Sep-09	J Alzheimers Dis	http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease	Alzheimer's Disease	"331 cases, 368 controls"	NR	1p31.1	TTLL7	rs7539409-?	rs7539409	0.18	0.000001		NR	NR	"Illumima [~550,000]"	N
9/30/2009	19740415	Sha	9-Sep-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19740415?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis	Amyotrophic lateral sclerosis (interaction)	"276 Caucasian cases, 271 Caucasian controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [549,062]"	N
9/29/2009	19734902	Harold	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease	Alzheimer's disease	"3,941 European ancestry cases, 7,848 European ancestry controls"	"2,023 European ancestry cases, 2,340 European ancestry controls"	19q13.32	"APOE, TOMM40"	rs2075650-?	rs2075650	0.15	0		2.53	[2.37-2.71]	"Illumina [529,205]"	N
9/29/2009	19734902	Harold	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease	Alzheimer's disease	"3,941 European ancestry cases, 7,848 European ancestry controls"	"2,023 European ancestry cases, 2,340 European ancestry controls"	11q14.2	PICALM	rs3851179-?	rs3851179	0.63	1.00E-09		1.16	[1.11-1.22]	"Illumina [529,205]"	N
9/29/2009	19734902	Harold	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease	Alzheimer's disease	"3,941 European ancestry cases, 7,848 European ancestry controls"	"2,023 European ancestry cases, 2,340 European ancestry controls"	8p21.1	CLU	rs11136000-?	rs11136000	0.6	9.00E-10		1.16	[1.11-1.22]	"Illumina [529,205]"	N
9/29/2009	19734903	Lambert	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease	Alzheimer's disease	"2,032 French cases, 5,328 French controls"	"3,978 European cases, 3,297 European controls"	1q32.2	CR1	2-SNP haplotype	"rs3818361,rs6656401"	0.18	3.00E-10	(AA)	1.22	[1.15-1.30]	"Illumina [537,029]"	N
9/29/2009	19734903	Lambert	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease	Alzheimer's disease	"2,032 French cases, 5,328 French controls"	"3,978 European cases, 3,297 European controls"	19q13.32	APOE	rs2075650-?	rs2075650	0.9	2.00E-16		NR	NR	"Illumina [537,029]"	N
9/29/2009	19734903	Lambert	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease	Alzheimer's disease	"2,032 French cases, 5,328 French controls"	"3,978 European cases, 3,297 European controls"	8p21.1	CLU	3-SNP haplotype	"rs2279590,rs11136000,rs9331888"	0.26	6.00E-10	(CCG)	1.22	[1.14-1.29]	"Illumina [537,029]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.68	8.00E-08		1.16	[1.10-1.22]	"Illumina [392,365]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	10q25.2	TCF7L2	rs7903146-T	rs7903146	0.27	1.00E-30		1.48	[1.39-1.57]	"Illumina [392,365]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	6p22.3	CDKAL1	rs4712523-G	rs4712523	0.32	2.00E-12		1.2	[1.14-1.26]	"Illumina [392,365]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	5q14.3	"LOC72901, CETN3"	rs12518099-C	rs12518099	0.23	7.00E-07		1.16	[1.10-1.22]	"Illumina [392,365]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	4p16.1	"WFS1, PPP2R2C"	rs4689388-T	rs4689388	0.57	1.00E-08		1.16	[1.10-1.21]	"Illumina [392,365]"	N
9/29/2009	19734900	Rung	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia"	Type 2 diabetes and other traits	"679 French cases, 697 French controls"	"5,579 European cases, 7,096 European controls"	2q36.3	"LOC64673, IRS1"	rs2943641-C	rs2943641	0.63	9.00E-12		1.19	[1.13-1.25]	"Illumina [392,365]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	Xp22.32	NR	rs5916687-?	rs5916687	0.27	0.000003		1.22	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	11q22.1	NR	rs2405657-?	rs2405657	0.66	0.000003		1.19	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	9p21.2	NR	rs774359-?	rs774359	0.25	0.000003		1.19	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	9p21.2	"MOBKL2B, IFNK, C9orf72"	rs2814707-?	rs2814707	0.23	7.00E-09		1.22	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	12p12.3	NR	rs9971637-?	rs9971637	0.05	0.000002		1.48	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	Xq13.3	NR	rs5937496-?	rs5937496	0.13	6.00E-07		1.38	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	19p13.11	UNC13A	rs12608932-?	rs12608932	0.34	3.00E-14		1.25	[NR]	"Illumina [292,768]"	N
9/29/2009	19734901	van Es	6-Sep-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"2,323 European descent cases, 9,013 European descent controls"	"2,532 European descent cases, 5,940 European descent controls"	9p21.2	"MOBKL2B, IFNK, C9orf72"	rs3849942-?	rs3849942	0.23	1.00E-08		1.23	[NR]	"Illumina [292,768]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	17q21.32	Intergenic	rs2326017-?	rs2326017	0.3	3.00E-07	(SWM strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	1q32.1	MDM4	rs12143943-?	rs12143943	0.41	0.000005	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	14q23.2	MTHFD1	rs10498514-?	rs10498514	0.02	8.00E-07	(SWM strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3q27.2	EHHADH	rs7374394-?	rs7374394	0.2	0.000002	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	18q22.1	"C18orf4, DSEL"	rs2124349-?	rs2124349	0.05	0.000004	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3q26.32	Intergenic	rs7612209-?	rs7612209	0.4	0.000004	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	1p32.1	JUN	rs4601609-?	rs4601609	0.05	0.000005	(PRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	7q31.1	IMMP2L	rs12531640-?	rs12531640	0.13	0.000006	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	7p14.1	VPS41	rs11984145-?	rs11984145	0.05	0.000006	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	Xp22.2	HCCS	rs5934953-?	rs5934953	0.02	1.00E-07	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	21q21.3	JAM2	rs17001239-?	rs17001239	0.12	0.000002	(PRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	1q23.2	VANGL2	rs16832015-?	rs16832015	0.01	0.000002	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	8q12.1	TOX	rs960089-?	rs960089	0.07	0.000006	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	9p22.2	SH3GL2	rs10810865-?	rs10810865	0.13	0.000004	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	11q14.2	C11orf73	rs6592284-?	rs6592284	0.21	0.000002	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	11p12	API5	rs10501293-?	rs10501293	0.25	0.000005	(SWM Strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	12q24.23	CCDC64	rs11064994-?	rs11064994	0.06	0.000006	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	13q14.11	DNAJC15	rs1324015-?	rs1324015	0.42	0.000009	(PC1)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	14q23.2	MTHFD1	rs2295639-?	rs2295639	0.02	0.000005	(SWM Strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	16q23.3	Intergenic	rs4082514-?	rs4082514	0.03	0.000003	(PC1)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	17q25.2	SEC14L1	rs3744064-?	rs3744064	0.03	7.00E-07	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	20p12.3	PLCB1	rs6056209-?	rs6056209	0.43	0.000002	(RVP)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	2q31.1	GORASP2	rs4668356-?	rs4668356	0.06	0.000001	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3p22.3	ARPP-21	rs6799705-?	rs6799705	0.05	2.00E-07	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3p25.1	GRIP2	rs9036-?	rs9036	0.19	0.000003	(PAL6)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	5p15.31	Intergenic	rs7729273-?	rs7729273	0.2	0.000001	(SSP)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	7q31.1	IMMP2L	rs10279573-?	rs10279573	0.14	0.000003	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	7p15.1	CPVL	rs2252521-?	rs2252521	0.34	0.000005	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	1q41	FAM177B	rs6683071-?	rs6683071	0.2	0.000004	(PC1)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	18q12.3	RIT2	rs8085804-?	rs8085804	0.37	0.000008	(VRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	15q23	CORO2B	rs11856323-?	rs11856323	0.08	1.00E-07	(PAL8)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	15q12	GABRB3	rs8043440-?	rs8043440	0.17	0.000002	(SRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	21q11.2	NRIP1	rs2229741-?	rs2229741	0.47	6.00E-07	(SRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	6p21.2	C6orf129	rs904251-?	rs904251	0.38	0.000007	(SWM Strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	8q24.13	FAM91A1	rs10481151-?	rs10481151	0.14	4.00E-07	(PRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	19q12	TSHZ3	rs1078373-?	rs1078373	0.37	0.000006	(SSP)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	12p13.1	GRIN2B	rs2160519-?	rs2160519	0.06	0.000002	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	11q13.5	CAPN5	rs3781684-?	rs3781684	0.11	0.000007	(VRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3q13.33	FBXO40	rs3772130-?	rs3772130	0.23	0.000006	(PC1)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	3p22.1	MOBP	rs816488-?	rs816488	0.04	0.000004	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	4q28.1	FAT4	rs12639834-?	rs12639834	0.36	0.000006	(SWM Strategy)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	16p12.1	Intergenic	rs2203512-?	rs2203512	0.14	3.00E-07	(PRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	Xp22.31	VCX3B	rs7892812-?	rs7892812	0.47	0.000008	(SSP)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	1p36.13	FAM131C	rs9442235-?	rs9442235	0.42	0.000006	(PC1)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	13q12.3	FLT1	rs17086609-?	rs17086609	0.35	0.000005	(IED)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	15q21.3	UNC13C	rs1897031-?	rs1897031	0.18	0.000001	(PRM)	NR	NR	"Illumina [475,971]"	N
10/2/2009	19734545	Need	4-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery	Cognitive performance	"1,295 individuals"	NR	13q34	Intergenic	rs767210-?	rs767210	0.11	3.00E-07	(PAL6)	NR	NR	"Illumina [475,971]"	N
9/28/2009	19729612	Paterson	3-Sep-09	Arterioscler Thromb Vasc Biol	http://www.ncbi.nlm.nih.gov/pubmed/19729612?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Identifies the ABO Blood Group as a Major Locus Associated With Serum Levels of Soluble E-Selectin	Serum soluble E-selectin	685 individuals with type 1 diabetes	477 nondiabetic siblings	9q34.2	ABO	rs579459-C	rs579459	0.2	1.00E-29		NR	NR	"Illumina [~841,000]"	N
9/28/2009	19729412	Tonjes	3-Sep-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19729412?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variation in GPR133 is Associated with Height - Genome Wide Association Study in the Self-contained Population of Sorbs	Height	"929 Sorbian individuals, 2,986 Caucasian individuals"	"2,772 German individuals"	12q24.33	GPR133	rs1569019-?	rs1569019	NR	5.00E-08		0.95	[0.61-1.29] cm increase	"Affymetrix [390,619]"	N
9/28/2009	19727025	De Moor	2-Sep-09	Med Sci Sports Exerc	http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults	Exercise (leisure time)	"1,644 Dutch individuals, 978 European individuals"	NR	10q23.2	PAPSS2	rs10887741-T	rs10887741	NR	0.000004		1.32	[1.17-1.49]	Affymetrix and Perlegen [~1.6 million] (imputed)	N
9/28/2009	19727025	De Moor	2-Sep-09	Med Sci Sports Exerc	http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults	Exercise (leisure time)	"1,644 Dutch individuals, 978 European individuals"	NR	18p11.32	C18orf2	rs8097348-G	rs8097348	NR	0.000007		1.36	[1.19-1.56]	Affymetrix and Perlegen [~1.6 million] (imputed)	N
9/28/2009	19727025	De Moor	2-Sep-09	Med Sci Sports Exerc	http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults	Exercise (leisure time)	"1,644 Dutch individuals, 978 European individuals"	NR	2q33.1	DNAPTP6	rs12612420-A	rs12612420	NR	0.000008		1.43	[1.22-1.67]	Affymetrix and Perlegen [~1.6 million] (imputed)	N
9/29/2009	19736353	Ising	1-Sep-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19736353?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression	Response to antidepressant treatment	339 German individuals	"1,193 German individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [389,251] (pooled)"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	6p21.33	Intergenic	rs12526186-?	rs12526186	NR	0.000003	(risperidone)	9	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	15q13.3	TRPM1	rs17815774-?	rs17815774	NR	0.000003	(risperidone)	9	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	1q21.3	Intergenic	rs10888501-?	rs10888501	NR	0.000001	(olanzapine)	9	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	3q28	Intergenic	rs7635839-?	rs7635839	NR	0.000003	(olanzapine)	9	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	2q14.3	CNTNAP5	rs17727261-?	rs17727261	NR	5.00E-07	(risperidone)	10	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	6p24.1	Intergenic	rs1040994-?	rs1040994	NR	0.000002	(olanzapine)	9	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	4p15.1	Intergenic	rs17390445-?	rs17390445	NR	1.00E-07	(ziprasidone)	17	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	9q33.3	Intergenic	rs888219-?	rs888219	NR	2.00E-07	(risperidone)	11	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/28/2009	19721433	McClay	1-Sep-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics	Treatment response to antipsychotics	738 cases	NR	12q23.1	ANKS1B	rs7968606-?	rs7968606	NR	3.00E-07	(olanzapine)	10	[NR] % of variance explained	"Affymetrix & Perlegen [492,900]"	N
9/10/2009	19723657	Spain	1-Sep-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19723657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Colorectal Cancer Risk Is Not Associated with Increased Levels of Homozygosity in a Population from the United Kingdom	Colorectal cancer	"921 white cases, 929 white controls"	"1,214 white cases, 1,435 white controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [486,303]"	N
9/9/2009	19724244	Laje	31-Aug-09	Pharmacogenet Genomics	http://www.ncbi.nlm.nih.gov/pubmed/19724244?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of suicidal ideation emerging during citalopram treatment of depressed outpatients	Response to antidepressant treatment	"90 white cases, 90 white controls"	"30 white cases, 1,652 white controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [100,864]"	N
9/9/2009	19714205	Hancock	28-Aug-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19714205?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children	Asthma (childhood onset)	492 Mexican trios	177 Mexican trios	9q21.31	"TLE4, CHCHD9"	rs2378383-?	rs2378383	0.78	7.00E-07		1.64	[1.32-2.04]	"Illumina [520,767]"	N
9/24/2009	19714249	Liu	28-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19714249?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males	Obesity and osteoporosis	"499 Caucasian males, 501 Caucasian females"	"1,370 Caucasian males, 1,985 Caucasian females"	11p15.1	SOX6	rs4756846-T	rs4756846	0.12	5.00E-07	"(BMI-BMD, males)"	NR	NR	"Affymetrix [379,319]"	N
9/24/2009	19714249	Liu	28-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19714249?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males	Obesity and osteoporosis	"499 Caucasian males, 501 Caucasian females"	"1,370 Caucasian males, 1,985 Caucasian females"	11p15.1	SOX6	rs297325-T	rs297325	0.23	4.00E-07	"(BMI-BMD, males)"	NR	NR	"Affymetrix [379,319]"	N
9/9/2009	19706858	Shuldiner	26-Aug-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19706858?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy	Response to clopidogrel therapy	429 Amish individuals	"140 white, 83 African American, and 4 unspecified individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [400,230]"	N
9/9/2009	19698717	Cui	18-Aug-09	Gastroenterology	http://www.ncbi.nlm.nih.gov/pubmed/19698717?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk	Esophageal cancer	"188 Japanese cases, 938 Japanese controls"	"699 Japanese cases, 1,482 Japanese controls"	4q23	"ADH6, ADH1B"	rs1229984-G	rs1229984	0.35	8.00E-24		1.79	[1.69-1.88]	"Illumina [359,195]"	N
9/9/2009	19698717	Cui	18-Aug-09	Gastroenterology	http://www.ncbi.nlm.nih.gov/pubmed/19698717?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk	Esophageal cancer	"188 Japanese cases, 938 Japanese controls"	"699 Japanese cases, 1,482 Japanese controls"	12q24.12	"BRAP, ALDH2"	rs671-A	rs671	0.36	3.00E-24		1.67	[1.58-1.76]	"Illumina [359,195]"	N
9/9/2009	19684573	Ge	16-Aug-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance	Response to Hepatitis C treatment	"871 Caucasian, 191 African American, and 75 Hispanic participants"	NR	4q34.3	Intergenic	rs17067123-?	rs17067123	NR	0.000008	(combined)	NR	NR	"Illumina [565,759]"	N
9/9/2009	19684573	Ge	16-Aug-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance	Response to Hepatitis C treatment	"871 Caucasian, 191 African American, and 75 Hispanic participants"	NR	19q13.2	IL28B	rs12979860-C	rs12979860	0.72	1.00E-28	(combined)	2	[1.8-2.3] (European-Americans)	"Illumina [565,759]"	N
9/9/2009	19684573	Ge	16-Aug-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance	Response to Hepatitis C treatment	"871 Caucasian, 191 African American, and 75 Hispanic participants"	NR	6q21	AKD2	rs9400317-?	rs9400317	NR	0.000007	(combined)	NR	NR	"Illumina [565,759]"	N
9/4/2009	19684604	Papaemmanuil	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia"	Acute lymphoblastic leukemia (childhood)	"503 European pediatric cases, 1,438 European pediatric controls"	"404 European pediatric cases, 960 European pediatric controls"	10q21.2	ARID5B	rs7089424-C	rs7089424	0.34	7.00E-19		1.65	[1.54-1.76]	"Illumina [291,473]"	N
9/4/2009	19684604	Papaemmanuil	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia"	Acute lymphoblastic leukemia (childhood)	"503 European pediatric cases, 1,438 European pediatric controls"	"404 European pediatric cases, 960 European pediatric controls"	14q11.2	CEBPE	rs2239633-G	rs2239633	0.52	3.00E-07		1.34	[1.22-1.45]	"Illumina [291,473]"	N
9/4/2009	19684604	Papaemmanuil	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia"	Acute lymphoblastic leukemia (childhood)	"503 European pediatric cases, 1,438 European pediatric controls"	"404 European pediatric cases, 960 European pediatric controls"	7p12.2	IKZF1	rs4132601-C	rs4132601	0.28	1.00E-19		1.69	[1.58-1.81]	"Illumina [291,473]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	12p13.32	C12orf5	rs10849033-G	rs10849033	0.02	0.000009		2.55	[1.60-3.80]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	1q43	RYR2	rs7554607-A	rs7554607	0.56	0.000002		1.49	[1.20-1.70]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	19q13.31	ZNF230	rs2191566-G	rs2191566	0.28	4.00E-07		1.52	[1.20-1.70]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	6q24.1	Intergenic	rs11155133-G	rs11155133	0.01	3.00E-07		3.62	[2.10-6.00]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	12q24.22	KRTHB5	rs2089222-A	rs2089222	0.03	8.00E-08		2.26	[1.60-3.0]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	7p12.2	"IKZF1, DDC"	rs11978267-G	rs11978267	0.27	8.00E-11		1.69	[1.40-1.90]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	10q21.2	ARID5B	rs10821936-C	rs10821936	0.34	1.00E-15		1.91	[1.60-2.20]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	18p11.32	Intergenic	rs1879352-C	rs1879352	0.16	0.000009		1.53	[1.20-1.80]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	10p11.21	PARD3	rs563507-A	rs563507	0.04	0.000009		2	[1.40-2.70]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	1p31.1	SIAT7C	rs10873876-T	rs10873876	0.15	0.000004		1.55	[1.20-1.80]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	3q26.32	KCNMB2	rs9290663-T	rs9290663	0.13	0.000006		1.58	[1.20-1.90]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	1q31.3	Intergenic	rs6428370-G	rs6428370	0.32	0.000007		1.43	[1.20-1.60]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	1q44	OR2C3	rs1881797-C	rs1881797	0.18	0.000007		1.52	[1.20-1.80]	"Affymetrix [307,944]"	N
9/11/2009	19684603	Trevino	16-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Germline genomic variants associated with childhood acute lymphoblastic leukemia	Acute lymphoblastic leukemia (childhood)	"317 European descent cases, 17,958 European descent controls"	NR	2q36.1	KCNE4	rs12621643-T	rs12621643	0.28	0.000003		1.48	[1.20-1.70]	"Affymetrix [307,944]"	N
9/4/2009	19680635	Alkelai	13-Aug-09	Psychopharmacology	http://www.ncbi.nlm.nih.gov/pubmed/19680635?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients	Response to antipsychotic treatment	"199 cases, 198 controls"	NR	2q24.3	FIGN	rs12476047-C	rs12476047	NR	0.000003		3.21	[1.97-5.25]	"Affymetrix & Perlegen [495,172]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	1q21.3	"AL157404.18, S100A5"	rs4845552-?	rs4845552	NR	0.000006		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	14q22.1	"FRMD6, AL079307.7"	rs11626056-?	rs11626056	NR	0.000001		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	20q11.23	C20orf132	rs8115854-?	rs8115854	NR	0.000002		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	20q11.23	RPN2	rs6031882-?	rs6031882	NR	0.000006		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	20q13.31	ZBP1	rs2073145-?	rs2073145	NR	0.000002		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	21q21.1	FDPSP	rs1888414-?	rs1888414	NR	2.00E-07		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	5q14.1	"AC104108.3, SCAMP1, LHFPL2"	rs6881634-?	rs6881634	NR	0.000002		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	5p14.1	Intergenic	rs7727656-?	rs7727656	NR	0.000008		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	5p15.1	AC026790.5	rs682748-?	rs682748	NR	0.000008		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	5q21.3	EFNA5	rs10074258-?	rs10074258	NR	2.00E-07		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	11q24.3	Intergenic	rs6590322-?	rs6590322	NR	0.000009		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	9q21.31	"RP11, 232A1.1"	rs10867752-?	rs10867752	NR	0.000003		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	9q21.13	PRUNE2	rs10781380-?	rs10781380	NR	7.00E-07		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	7p21.3	Intergenic	rs9918508-?	rs9918508	NR	0.000008		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	5q14.1	ARSB	rs337847-?	rs337847	NR	0.000007		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	12q13.11	"ARID2, SFRS2IP"	rs1373549-?	rs1373549	NR	0.000008		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	12q14.3	CAND1	rs1082714-?	rs1082714	NR	0.000005		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	7p12.2	"IKZF1, AC020743.7"	rs10276619-?	rs10276619	NR	0.000003		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	7q21.11	MAGI2	rs11525066-?	rs11525066	NR	0.000003		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	13q31.1	Intergenic	rs4773460-?	rs4773460	NR	0.000002		NR	NR	"Illumina [516,645]"	N
9/9/2009	19668339	Potkin	7-Aug-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease	Hippocampal atrophy	"172 cases, 209 controls"	NR	8q24.12	MAL2	rs1364705-?	rs1364705	NR	0.000009		NR	NR	"Illumina [516,645]"	N
9/4/2009	19664746	Tse	5-Aug-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.	Nasopharyngeal carcinoma	"277 Han Chinese cases, 285 Han Chinese controls"	"635 Han Chinese cases, 1,640 Han Chinese controls"	6p22.1	GABBR1	rs29232-A	rs29232	0.46	9.00E-17		1.67	[1.48-1.88]	"Illumina [480,365]"	N
9/4/2009	19664746	Tse	5-Aug-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.	Nasopharyngeal carcinoma	"277 Han Chinese cases, 285 Han Chinese controls"	"635 Han Chinese cases, 1,640 Han Chinese controls"	6p21.33	HLA-A	rs2517713-A	rs2517713	0.62	4.00E-20		1.88	[1.65-2.15]	"Illumina [480,365]"	N
9/4/2009	19664746	Tse	5-Aug-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.	Nasopharyngeal carcinoma	"277 Han Chinese cases, 285 Han Chinese controls"	"635 Han Chinese cases, 1,640 Han Chinese controls"	6p22.1	HLA-F	rs3129055-G	rs3129055	0.31	7.00E-11		1.51	[1.34-1.71]	"Illumina [480,365]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	5p15.33	CLPTM1L	rs4975616-?	rs4975616	NR	3.00E-09		1.15	[1.10-1.20]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	15q25.1	CHRNA3	rs8034191-?	rs8034191	NR	3.00E-26		1.29	[1.23-1.35]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	6p21.33	BAT3	rs3117582-?	rs3117582	NR	4.00E-10		1.24	[1.16-1.33]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	2p14	NR	rs4254535-?	rs4254535	NR	0.000005		1.12	[NR]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	15q15.2	TGM5	rs748404-?	rs748404	NR	0.000001		1.15	[1.09-1.20]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	3p24.1	NR	rs1530057-?	rs1530057	NR	0.000003		1.26	[NR]	"Illumina [511,919]"	N
9/14/2009	19654303	Broderick	4-Aug-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study	Lung cancer	"1,952 European cases, 1,438 European controls"	"5,608 European cases, 6,767 European controls"	10q23.31	NR	rs1926203-?	rs1926203	NR	0.000001		1.12	[NR]	"Illumina [511,919]"	N
9/4/2009	19651812	Chambers	3-Aug-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19651812?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type-2 diabetes amongst Indian Asians and European whites	Fasting plasma glucose	"7,474 Indian Asian individuals"	"4,462 European controls"	11q21	MTNR1B	rs2166706-G	rs2166706	0.46	2.00E-09		0.07	(0.04-0.09) mmol/L increase	"Illumina [up to 544,390]"	N
9/4/2009	19656524	Grant	3-Aug-09	J Pediatr	http://www.ncbi.nlm.nih.gov/pubmed/19656524?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24	Nonsyndromic cleft lip with or without cleft palate	"111 European ancestry cases, 5,951 European ancestry controls"	NR	8q24.21	Intergenic	rs987525-?	rs987525	0.22	9.00E-08		2.09	[1.59-2.76]	"Illumina [495,858]"	N
9/4/2009	19656524	Grant	3-Aug-09	J Pediatr	http://www.ncbi.nlm.nih.gov/pubmed/19656524?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24	Nonsyndromic cleft lip with or without cleft palate	"111 European ancestry cases, 5,951 European ancestry controls"	NR	18q22.3	Intergenic	rs17085106-?	rs17085106	0.018	4.00E-08		4.07	[2.37-7.00]	"Illumina [495,858]"	N
9/4/2009	19648918	Amundadottir	2-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19648918?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer	Pancreatic cancer	"1,771 European ancestry cases, 1,805 European ancestry controls"	"2,120 European ancestry cases, 2,127 European ancestry controls"	9q34.2	ABO	rs505922-T	rs505922	0.35	5.00E-08		1.2	[1.12-1.28]	"Illumina [558,542]"	N
9/4/2009	19648919	Song	2-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19648919?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2	Ovarian cancer	"1,817 European ancestry cases, 2,353 European ancestry controls"	"6,944 European ancestry cases, 9,477 European ancestry controls"	9p22.2	"BNC2, LOC648570, CNTLN"	rs3814113-T	rs3814113	0.68	5.00E-19		1.22	[1.16-1.27]	"Illumina [up to ~2,000,000] (imputed)"	N
8/21/2009	19648920	Wu	2-Aug-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19648920?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer	Bladder cancer	"969 Caucasian cases, 957 Caucasian controls"	"5,698 US and European cases, 38,633 US and European controls"	8q24.3	PSCA	rs2294008-T	rs2294008	0.46	2.00E-10		1.15	[1.10-1.20]	"Illumina [556,429]"	N
9/4/2009	19667218	Comabella	1-Aug-09	Arch Neurol	http://www.ncbi.nlm.nih.gov/pubmed/19667218?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis"	Response to interferon beta therapy	"53 responders, 53 non-responders"	"49 responders, 45 non-responders"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [428,867](pooled)"	N
8/21/2009	19625618	Nakano	22-Jul-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19625618?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population	Glaucoma (primary open-angle)	"418 Japanese cases, 300 Japanese controls"	"409 Japanese cases, 448 Japanese controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [331,838]"	N
8/21/2009	19620980	Skibola	20-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19620980?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics variants at 6p21.33 are associated with susceptibility to follicular lymphoma	Follicular lymphoma	"189 European ancestry cases, 592 European controls"	"456 European ancestry cases, 2,785 European ancestry controls"	6p21.33	"STG, PSORS1"	rs6457327-C	rs6457327	0.62	5.00E-11		1.69	[1.43-2.00]	"Illumina [~500,000] (pooled)"	N
8/12/2009	19609347	Adeyemo	17-Jul-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19609347?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans	Hypertension	"509 African American cases, 508 African American controls"	"366 West African cases, 614 West African controls"	15q22.1	ALDH1A2	rs1550576-?	rs1550576	0.86	0.000003		1.92	[NR]	"Affymetrix [808,465]"	N
8/12/2009	19609347	Adeyemo	17-Jul-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19609347?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans	Hypertension	"509 African American cases, 508 African American controls"	"366 West African cases, 614 West African controls"	4q23	ADH7	rs991316-T	rs991316	0.45	0.000005		1.62	[NR]	"Affymetrix [808,465]"	N
8/4/2009	19597492	Benjamin	13-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry	Atrial fibrillation	"3,413 cases, 37,105 referents"	"2,145 cases, 4,073 controls"	1p36.22	"MTHFR, NPPA"	rs17375901-T	rs17375901	0.053	6.00E-07		1.26		Affymetrix & Illumina [~2.5 million] (imputed)	N
8/4/2009	19597492	Benjamin	13-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry	Atrial fibrillation	"3,413 cases, 37,105 referents"	"2,145 cases, 4,073 controls"	16q22.3	ZFHX3	rs2106261-T	rs2106261	0.174	2.00E-15		1.25		Affymetrix & Illumina [~2.5 million] (imputed)	N
8/4/2009	19597492	Benjamin	13-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry	Atrial fibrillation	"3,413 cases, 37,105 referents"	"2,145 cases, 4,073 controls"	4q25	PITX2	rs17042171-A	rs17042171	0.12	4.00E-63		1.65		Affymetrix & Illumina [~2.5 million] (imputed)	N
7/30/2009	19597491	Gudbjartsson	13-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19597491?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke	Atrial fibrillation	"2,385 European cases, 33,752 European controls"	"up to 2,427 European cases, 3,379 European controls"	16q22.3	ZFHX3	rs7193343-T	rs7193343	NR	1.00E-10		1.21	[1.14-1.29]	"Illumina [303,136]"	N
7/30/2009	19597491	Gudbjartsson	13-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19597491?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke	Atrial fibrillation	"2,385 European cases, 33,752 European controls"	"up to 2,427 European cases, 3,379 European controls"	4q25	Intergenic	rs2200733-?	rs2200733	0.12	1.00E-14		1.42	[NR]	"Illumina [303,136]"	N
7/24/2009	19587794	Nolte	9-Jul-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19587794?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies	Cardiac repolarisation	"3,558 Caucasian individuals"	"29,527 Caucasian individuals"	6q22.31	"SLC35F1, C6orf204, PLN"	rs11153730-C	rs11153730	0.5	2.00E-29		0.09	[NR] unit increase	"Affymetrix & Illumina [~2,399,142] (imputed)"	N
7/24/2009	19587794	Nolte	9-Jul-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19587794?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies	Cardiac repolarisation	"3,558 Caucasian individuals"	"29,527 Caucasian individuals"	1q23.3	"OLFML2B, NOS1AP"	rs12143842-T	rs12143842	0.25	1.00E-83		0.18	[NR] unit increase	"Affymetrix & Illumina [~2,399,142] (imputed)"	N
7/24/2009	19584900	Tonjes	8-Jul-09	Eur J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19584900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany	Body mass index and fat mass	948 Sorbian individuals	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [390,619]"	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	12p12.2	PDE3A	rs10770612-G	rs10770612	0.19	2.00E-08		0.03	[0.02-0.04] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	12q14.3	HMGA2	rs4026608-C	rs4026608	0.38	2.00E-09		0.03	[0.02-0.04] cm decrease	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	15q24.1	LOXL1	rs893817-G	rs893817	0.34	0.000003		0.02	[0.01-0.03] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	5q23.2	"CCDC100, PPIC"	rs17470137-A	rs17470137	0.29	1.00E-11		0.03	[0.02-0.04] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	1p21.2	PALMD	rs7543130-A	rs7543130	0.49	1.00E-07		0.03	[0.02-0.04] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Aortic root size	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	17p13.3	"SMG6, SRR, TSR1, SGSM2"	rs10852932-T	rs10852932	0.36	2.00E-11		0.03	[0.02-0.04] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Cardiac structure and function	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	16q23.1	WWOX	rs2059238-A	rs2059238	0.22	0.000003	(LV wall thickness)	0.02	[0.01-0.03] cm decrease	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Cardiac structure and function	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	10q23.1	GRID1	rs7910620-G	rs7910620	0.01	7.00E-07	(LV wall thickness)	0.17	[0.11-0.23] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Cardiac structure and function	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	5q22.1	SLC25A46	rs17132261-T	rs17132261	0.02	9.00E-07	(LV wall thickness)	0.06	[0.04-0.08] cm increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
8/7/2009	19584346	Vasan	8-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data	Cardiac structure and function	"12,612 European ancestry individuals"	"4,094 European ancestry individuals"	6q22.31	"SLC35F1, C6orf204, PLN"	rs89107-G	rs89107	0.5	1.00E-09	(LV internal diastolic dimensions)	0.03	[0.02-0.04] cm decrease	Affymetrix & Illumina [~2.5 million] (imputed)	N
7/16/2009	19578364	Bishop	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies three loci associated with melanoma risk	Melanoma	"1,539 European ancestry cases, 3,917 European ancestry controls"	"2,312 European ancestry cases, 1,867 European ancestry controls"	16q24.3	MC1R	rs4785763-A	rs4785763	0.32	6.00E-22		1.36	[1.28-1.45]	"Illumina [~317,000]"	N
7/16/2009	19578364	Bishop	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies three loci associated with melanoma risk	Melanoma	"1,539 European ancestry cases, 3,917 European ancestry controls"	"2,312 European ancestry cases, 1,867 European ancestry controls"	9p21.3	CDKN2A	rs7023329-A	rs7023329	0.5	4.00E-07		1.18	[1.10-1.25]	"Illumina [~317,000]"	N
7/16/2009	19578364	Bishop	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies three loci associated with melanoma risk	Melanoma	"1,539 European ancestry cases, 3,917 European ancestry controls"	"2,312 European ancestry cases, 1,867 European ancestry controls"	11q14.3	TYR	rs1393350-A	rs1393350	0.27	2.00E-14		1.29	[1.21-1.38]	"Illumina [~317,000]"	N
7/16/2009	19578364	Bishop	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies three loci associated with melanoma risk	Melanoma	"1,539 European ancestry cases, 3,917 European ancestry controls"	"2,312 European ancestry cases, 1,867 European ancestry controls"	22q13.1	Intergenic	rs2284063-?	rs2284063	0.37	2.00E-09		1.2	[1.14-1.28]	"Illumina [~317,000]"	N
7/16/2009	19578364	Bishop	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies three loci associated with melanoma risk	Melanoma	"1,539 European ancestry cases, 3,917 European ancestry controls"	"2,312 European ancestry cases, 1,867 European ancestry controls"	16q24.3	MC1R	rs258322-A	rs258322	0.09	3.00E-27		1.67	[1.52-1.83]	"Illumina [~317,000]"	N
7/13/2009	19578365	Falchi	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578365?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi	Cutaneous nevi	"1,524 European twins"	"4,107 European individuals"	22q13.1	PLA2G6	rs2284063-G	rs2284063	0.35	3.00E-08		0.08	[-0.002-0.16] decrease in log nevus count	"Illumina [297,108]"	N
7/13/2009	19578365	Falchi	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578365?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi	Cutaneous nevi	"1,524 European twins"	"4,107 European individuals"	9p21.3	MTAP	rs4636294-A	rs4636294	0.48	3.00E-15		0.2	[0.13-0.27] increase in log nevus count	"Illumina [297,108]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	5p15.33	TERT	rs2736100-G	rs2736100	0.49	2.00E-17		1.27	[1.19-1.37]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	8q24.21	CCDC26	rs891835-G	rs10464870	0.78	8.00E-11		1.24	[1.17-1.30]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	20q13.33	RTEL1	rs6010620-G	rs6010620	0.23	3.00E-12		1.28	[1.21-1.35]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	9p21.3	"CDKN2A, CDKN2B"	rs4977756-G	rs4977756	0.6	7.00E-15		1.24	[1.19-1.30]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	8q24.21	CCDC26	rs4295627-G	rs4295627	0.83	2.00E-18		1.36	[1.29-1.43]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	5p15.33	TERT	rs2853676-A	rs2853676	0.73	4.00E-14		1.26	[1.20-1.32]	"Illumina [454,576]"	N
7/12/2009	19578367	Shete	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies five susceptibility loci for glioma	Glioma	"1,878 cases, 3,670 controls"	"2,545 cases, 2,953 controls"	11q23.3	PHLDB1	rs498872-T	rs498872	0.69	1.00E-08		1.18	[1.13-1.24]	"Illumina [454,576]"	N
7/12/2009	19578366	Wrensch	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility	Glioma (high-grade)	"692 high-grade cases, 3,992 controls"	"176 high-grade cases, 174 controls"	20q13.33	RTEL1	rs6010620-G	rs6010620	0.77	3.00E-09		1.52	[1.32-1.75]	"Illumina [326,506]"	N
7/12/2009	19578366	Wrensch	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility	Glioma (high-grade)	"692 high-grade cases, 3,992 controls"	"176 high-grade cases, 174 controls"	20q13.33	RTEL1	rs4809324-C	rs4809324	0.1	2.00E-09		1.6	[1.37-1.87]	"Illumina [326,506]"	N
7/12/2009	19578366	Wrensch	5-Jul-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility	Glioma (high-grade)	"692 high-grade cases, 3,992 controls"	"176 high-grade cases, 174 controls"	9p21.3	Intergenic	rs1412829-C	rs1412829	0.39	2.00E-10		1.42	[1.27-1.58]	"Illumina [326,506]"	N
7/24/2009	19578179	Teichert	4-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of acenocoumarol maintenance dosage	Acenocoumarol maintenance dosage	"1,451 Caucasian individuals"	287 Caucasian individuals	10q23.33	CYP2C18	rs12772169-?	rs12772169	NR	8.00E-12		NR	NR	"Illumina [~550,000]"	N
7/24/2009	19578179	Teichert	4-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of acenocoumarol maintenance dosage	Acenocoumarol maintenance dosage	"1,451 Caucasian individuals"	287 Caucasian individuals	3q22.3	CNTN4	rs10935268-?	rs10935268	NR	8.00E-07		NR	NR	"Illumina [~550,000]"	N
7/24/2009	19578179	Teichert	4-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of acenocoumarol maintenance dosage	Acenocoumarol maintenance dosage	"1,451 Caucasian individuals"	287 Caucasian individuals	19p13.12	CYP4F2	rs2108622-?	rs2108622	NR	3.00E-10		NR	NR	"Illumina [~550,000]"	N
7/24/2009	19578179	Teichert	4-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of acenocoumarol maintenance dosage	Acenocoumarol maintenance dosage	"1,451 Caucasian individuals"	287 Caucasian individuals	10q23.33	CYP2C19	rs12767583-?	rs12767583	NR	3.00E-07		NR	NR	"Illumina [~550,000]"	N
7/12/2009	19567438	Elliott	1-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease	C-reactive protein	"17,967 European and Indian Asian men and women"	"13,615 European and Indian Asian men and women"	1q23.2	CRP	rs7553007-A	rs7553007	NR	8.00E-44		20.7	[18.9-23.4] % decrease	"Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)"	N
7/12/2009	19567438	Elliott	1-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease	C-reactive protein	"17,967 European and Indian Asian men and women"	"13,615 European and Indian Asian men and women"	1q21.3	IL6R	rs4537545-T	rs4537545	NR	2.00E-14		11.5	[8.5-14.4] % decrease	"Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)"	N
7/12/2009	19567438	Elliott	1-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease	C-reactive protein	"17,967 European and Indian Asian men and women"	"13,615 European and Indian Asian men and women"	19q13.32	"APOE, APOCI, APOCII"	rs4420638-G	rs4420638	NR	5.00E-27		21.8	[18.1-25.3] % decrease	"Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)"	N
7/12/2009	19567438	Elliott	1-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease	C-reactive protein	"17,967 European and Indian Asian men and women"	"13,615 European and Indian Asian men and women"	1p31.3	LEPR	rs6700896-T	rs6700896	NR	3.00E-14		14.8	[12.0-17.6] % decrease	"Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)"	N
7/12/2009	19567438	Elliott	1-Jul-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease	C-reactive protein	"17,967 European and Indian Asian men and women"	"13,615 European and Indian Asian men and women"	12q24.31	HNF1A	rs1183910-T	rs1183910	NR	1.00E-30		13.8	[10.9-16.6] % decrease	"Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)"	N
7/24/2009	19570815	Estrada	1-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation	Height	"10,074 European individuals"	"6,912 European individuals"	22q13.1	"SGSM3, MKL1"	rs5757949-T	rs5757949	NR	0.000004		NR	NR	"Affymetrix, Illumina & Perlegen [2,228,850] (imputed)"	N
7/24/2009	19570815	Estrada	1-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation	Height	"10,074 European individuals"	"6,912 European individuals"	2q37.1	"DIS3L2, ALPP, NPPC"	rs6717918-T	rs6717918	0.78	3.00E-09		0.44	[0.20-0.68] cm increase	"Affymetrix, Illumina & Perlegen [2,228,850] (imputed)"	N
7/24/2009	19570815	Estrada	1-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation	Height	"10,074 European individuals"	"6,912 European individuals"	11q14.1	"TMEM126B, TMEM126A"	rs10898392-T	rs10898392	NR	0.000003		NR	NR	"Affymetrix, Illumina & Perlegen [2,228,850] (imputed)"	N
7/24/2009	19570815	Estrada	1-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation	Height	"10,074 European individuals"	"6,912 European individuals"	5p13.3	"C5orf23, NPR3"	rs10472828-C	rs10472828	0.56	3.00E-07		0.22	[0.04-0.40] cm increase	"Affymetrix, Illumina & Perlegen [2,228,850] (imputed)"	N
7/24/2009	19570815	Estrada	1-Jul-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation	Height	"10,074 European individuals"	"6,912 European individuals"	22q13.1	"TNRC6B, ADSL"	rs139909-T	rs139909	0.68	2.00E-07		0.25	[0.03-0.47] cm increase	"Affymetrix, Illumina & Perlegen [2,228,850] (imputed)"	N
7/13/2009	19571811	International Schizophrenia Consortium	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder	Schizophrenia	"3,322 European descent cases, 3,587 European descent controls"	"4,692 European descent cases, 15,493 European descent controls"	18q21.2	TCF4	rs17594526-T	rs17594526	0.03	1.00E-07		1.44		"Affymetrix [739,995]"	N
7/13/2009	19571811	International Schizophrenia Consortium	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder	Schizophrenia	"3,322 European descent cases, 3,587 European descent controls"	"4,692 European descent cases, 15,493 European descent controls"	1p21.3	PTBP2	rs7544736-G	rs7544736	0.18	6.00E-07		1.25		"Affymetrix [739,995]"	N
7/13/2009	19571811	International Schizophrenia Consortium	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder	Schizophrenia	"3,322 European descent cases, 3,587 European descent controls"	"4,692 European descent cases, 15,493 European descent controls"	3q26.33	FXR1	rs6782299-T	rs6782299	0.73	1.00E-07		1.1		"Affymetrix [739,995]"	N
7/13/2009	19571811	International Schizophrenia Consortium	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common polygenic variation contributes to risk of schizophrenia and bipolar disorder	Schizophrenia	"3,322 European descent cases, 3,587 European descent controls"	"4,692 European descent cases, 15,493 European descent controls"	6p22.1	MHC	rs13194053-T	rs13194053	0.86	1.00E-08		1.22		"Affymetrix [739,995]"	N
7/10/2009	19571809	Shi	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571809?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on chromosome 6p22.1 are associated with schizophrenia	Schizophrenia	"2,681 European ancestry cases, 2,653 European ancestry controls, 1,286 African American cases, 973 African American controls"	"5,327 European ancestry cases, 16,424 European ancestry controls"	6p22.1	"SLC17A1, SLC17A3, BTN3A2, BTN2A2, BTN3A1, HIST1H2AG, HIST1H2BJ, PRSS16, POM121L2, ZNF184"	rs13194053-T	rs13194053	0.82	1.00E-08	(EA)	1.28	[NR]	"Affymetrix [up to 843,798]"	N
7/10/2009	19571809	Shi	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571809?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on chromosome 6p22.1 are associated with schizophrenia	Schizophrenia	"2,681 European ancestry cases, 2,653 European ancestry controls, 1,286 African American cases, 973 African American controls"	"5,327 European ancestry cases, 16,424 European ancestry controls"	6p21.32	HLA-DQA1	rs9272219-G	rs9272219	0.72	7.00E-08	(EA)	1.14	[NR]	"Affymetrix [up to 843,798]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	5q21.1	SLCO6A1	rs1502844-C	rs1502844	NR	0.000001		1.09	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	2p16.1	VRK2	rs2312147-C	rs2312147	NR	3.00E-07		1.09	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	18q21.2	TCF4	rs9960767-C	rs9960767	0.06	4.00E-09		1.23	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	6p21.32	"MHC, NOTCH4"	rs3131296-G	rs3131296	0.87	2.00E-10		1.19	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	9q33.1	Intergenic	rs1572299-A	rs1572299	NR	0.000004		1.08	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	11q24.2	NRGN	rs12807809-T	rs12807809	0.83	2.00E-09		1.15	[NR]	"Illumina [314,868]"	N
7/10/2009	19571808	Stefansson	1-Jul-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants conferring risk of schizophrenia	Schizophrenia	"2,663 European cases, 13,498 European controls"	"10,282 European cases, 21,093 European controls"	6p22.1	"MHC, PRSS16"	rs6932590-T	rs6932590	0.78	1.00E-12		1.16	[NR]	"Illumina [314,868]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	5q32	PPP2R2B	rs1864982-A	rs1864982	0.13	0.000003		1.36	[1.20-1.55]	"Illumina [524,396]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	6q25.1	ESR1	rs6902771-C	rs6902771	0.51	0.000008		1.24	[1.13-1.36]	"Illumina [524,396]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	Xp22.2	Intergenic	rs12388359-T	rs12388359	0.11	0.000004		1.61	[1.32-2.00]	"Illumina [524,396]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	2q35	PECR	rs7590720-G	rs7590720	0.29	1.00E-08		1.35	[1.22-1.49]	"Illumina [524,396]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	4q26	"CAST, ERAP1"	rs13150562-G	rs13150562	0.68	0.000007		1.27	[1.14-1.41]	"Illumina [524,396]"	N
7/24/2009	19581569	Treutlein	1-Jul-09	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of alcohol dependence	Alcohol dependence	"476 German cases, 1,358 German controls"	"1,024 German cases, 996 German controls"	14q24.2	Intergenic	rs36563-A	rs36563	0.15	0.000005		1.33	[1.18-1.50]	"Illumina [524,396]"	N
7/1/2009	19561606	Thorleifsson	28-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19561606?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density	Kidney stones	"1,507 Icelandic cases, 34,033 Icelandic controls"	"1,520 Icelandic cases, 4,726 Icelandic controls, 746 Dutch cases, 3,751 Dutch controls"	21q22.13	CLDN14	rs219780-C	rs219780	0.79	4.00E-12		1.25	[1.17-1.33]	"Illumina [303,120]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	16q12.2	FTO	rs1558902-?	rs1558902	NR	5.00E-19		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	6p12.2	PKHD1	rs1555967-?	rs1555967	NR	0.000003		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	12q13.13	"FAIM2, BCDIN3D"	rs7138803-?	rs7138803	NR	8.00E-07		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	11p15.4	OVCH2	rs7932813-?	rs7932813	NR	0.000005		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	18q21.32	MC4R	rs489693-?	rs489693	NR	4.00E-07		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	14q31.1	NRXN3	rs10146997-G	rs10146997	NR	5.00E-08		0.65	[NR] cm increase	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557197	Heard-Costa	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium	Waist circumference	"31,373 Caucasian individuals"	"38,641 Caucasian individuals"	5p14.3	CDH12	rs4701252-?	rs4701252	NR	0.000002		NR	NR	"Affymetrix & Illumina [up to 512,349]"	N
7/1/2009	19557161	Lindgren	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution	Adiposity	"38,580 European-ancestry individuals"	"Up to 102,064 European-ancestry individuals"	6p12.3	TFAP2B	rs987237-G	rs987237	0.164	2.00E-11	(WC)	0.04	[0.03-0.05] z-score unit increase	"Affymetrix & Illumina [2,573,738] (imputed)"	N
7/1/2009	19557161	Lindgren	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution	Adiposity	"38,580 European-ancestry individuals"	"Up to 102,064 European-ancestry individuals"	1q42.3	TBCE	rs6429082-C	rs6429082	0.46	3.00E-07	(WC)	NR	NR	"Affymetrix & Illumina [2,573,738] (imputed)"	N
7/1/2009	19557161	Lindgren	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution	Adiposity	"38,580 European-ancestry individuals"	"Up to 102,064 European-ancestry individuals"	1q41	LYPLAL1	rs2605100-G	rs2605100	0.692	3.00E-08	(WHR in women)	0.04	[0.03-0.05] z-score unit increase	"Affymetrix & Illumina [2,573,738] (imputed)"	N
7/1/2009	19557161	Lindgren	26-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution	Adiposity	"38,580 European-ancestry individuals"	"Up to 102,064 European-ancestry individuals"	8p23.1	MSRA	rs7826222-G	rs7826222	0.183	9.00E-09	(WC)	0.04	[0.03-0.05] z-score unit increase	"Affymetrix & Illumina [2,573,738] (imputed)"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	4q26	TRAM1L1	rs10433903-T	rs10433903	0.66	0.000003		1.33	[1.19-1.52]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	2p16.1	RTN4	rs6726292-G	rs6726292	0.73	0.000001		1.39	[1.22-1.59]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	10q22.1	PRF1	rs10999409-T	rs10999409	0.45	0.000005		1.3	[1.16-1.45]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	10p11.21	ZNF248	rs7474896-T	rs7474896	0.14	9.00E-07		1.46	[1.25-1.69]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	6p21.31	ITPR3	rs999943-T	rs999943	0.72	0.000001		1.37	[1.20-1.56]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	6p21.31	MLN	rs2274459-A	rs2274459	0.17	0.000006		1.38	[1.20-1.58]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	11p14.2	MUC15	rs12295638-C	rs12295638	0.1	0.000004		1.49	[1.26-1.77]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	16q12.2	FTO	rs9941349-T	rs9941349	0.43	6.00E-12		1.48	[1.33-1.66]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	3p24.3	RAFTLIN	rs12635698-C	rs12635698	0.15	0.000005		1.41	[1.21-1.63]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	3p24.2	RARB	rs1435703-T	rs1435703	0.06	0.000004		1.66	[1.34-2.06]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	20p12.1	C20orf133	rs6110577-C	rs6110577	0.16	0.000005		1.4	[1.21-1.61]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	5q23.3	FBN2	rs374748-G	rs374748	0.11	0.000004		1.47	[1.25-1.73]	"Illumina [457,251]"	N
7/1/2009	19553259	Cotsapas	24-Jun-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common BMI-associated variants confer risk of extreme obesity	Obesity (extreme)	"775 Caucasian cases, 3,197 Caucasian controls"	NR	2q33.3	FLJ20309	rs7603514-A	rs7603514	0.2	0.000008		1.36	[1.19-1.56]	"Illumina [457,251]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	20q13.12	CD40	rs6074022-G	rs6074022	0.25	1.00E-07		1.2	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	16p12.1	NR	rs8049603-T	rs8049603	0.2	0.000001		1.19	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	8q24.21	"ASAP1, DDEF1"	rs6984045-C	rs6984045	0.02	0.000002		1.59	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	10p15.1	IL2RA	rs2104286-G	rs2104286	0.73	0.000007		1.16	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	1p13.1	CD58	rs1335532-A	rs1335532	0.87	1.00E-07		1.28	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	1p22.1	"EVI5, RPL5"	rs6604026-G	rs6604026	0.28	0.000003		1.17	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	6p21.32	HLA-DRB1	rs9271366-G	rs9271366	0.15	0		2.78	[NR]	"Illumina [302,098]"	N
6/30/2009	19525955	Bahlo	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20	Multiple sclerosis	"1,618 European ancestry cases, 3,413 European ancestry controls"	"2,256 European ancestry cases, 2,310 European ancestry controls"	12q14.1	"METTL1, CYP27B1"	rs703842-A	rs703842	0.67	5.00E-11		1.23	[NR]	"Illumina [302,098]"	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	5p13.2	IL7R	rs6897932-C	rs6897932	0.75	0.000002		1.12	[1.02-1.23]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	2q22.1	CXCR4	rs882300-C	rs882300	0.61	1.00E-07		1.19	[1.09-1.30]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	12p13.31	TNFRSF1A	rs1800693-C	rs1800693	0.45	2.00E-11		1.2	[1.10-1.31]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	10p15.1	IL2RA	rs2104286-T	rs2104286	0.76	9.00E-08		1.15	[1.04-1.27]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	1p13.1	CD58	rs2300747-A	rs2300747	0.88	3.00E-10		1.3	[1.14-1.47]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	6p21.32	HLA-DRB1	rs3135388-A	rs3135388	0.22	0		2.75	[2.46-3.07]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	6p22.1	HLA-B	rs2523393-A	rs2523393	0.59	1.00E-17		1.28	[1.18-1.39]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	3q25.33	IL12A	rs4680534-C	rs4680534	0.37	0.000006		1.12	[1.02-1.22]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	10q22.3	ZMIZ1	rs1250540-G	rs1250540	0.35	0.000002		1.12	[1.02-1.22]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	12q24.31	MPHOSPH9	rs1790100-G	rs1790100	0.24	7.00E-07		1.11	[1.00-1.22]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	5p13.1	PTGER4	rs6896969-C	rs6896969	0.62	2.00E-07		1.1	[1.01-1.20]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	16p13.13	CLEC16A	rs11865121-C	rs11865121	0.69	2.00E-07		1.15	[1.04-1.25]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	12p13.31	TNFRSF1A	rs4149584-T	rs4149584	0.022	0.000005		1.58	[1.15-2.17]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	16q24.1	IRF8	rs17445836-G	rs17445836	0.81	4.00E-09		1.25	[1.12-1.39]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/29/2009	19525953	De Jager	14-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci"	Multiple sclerosis	"2,624 cases, 7,220 controls"	"2,215 cases, 2,116 controls"	11q12.2	CD6	rs17824933-G	rs17824933	0.25	4.00E-09		1.18	[1.07-1.30]	Affymetrix & Illumina [~2.56 million] (imputed)	N
6/26/2009	19525478	Malarstig	12-Jun-09	Blood	http://www.ncbi.nlm.nih.gov/pubmed/19525478?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study	Plasma homocysteine	387 individuals from 21 Spanish families	"1,238 European individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [283,437]"	N
6/19/2009	19508998	Knauff	9-Jun-09	Hum Reprod	http://www.ncbi.nlm.nih.gov/pubmed/19508998?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene	Premature ovarian failure	"99 Caucasian cases, 235 Caucasian controls"	"60 Caucasian cases, 90 Caucasian controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [309,158]"	N
6/19/2009	19508968	Zhai	8-Jun-09	J Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19508968?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium	Osteoarthritis	"1,804 Caucasian individuals"	"3,266 Caucasian individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [up to 535,188]"	N
6/17/2009	19503088	Gregersen	7-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis"	Rheumatoid arthritis	"2,418 cases, 4,504 controls"	"2,604 cases, 2,882 controls"	2p16.1	REL	rs13017599-A	rs13017599	0.34	2.00E-12		1.21	[1.15-1.28]	"Illumina [278,502]"	N
6/17/2009	19503088	Gregersen	7-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis"	Rheumatoid arthritis	"2,418 cases, 4,504 controls"	"2,604 cases, 2,882 controls"	2q33.2	CTLA4	rs231735-T	rs231735	0.51	6.00E-09		1.17	[1.11-1.23]	"Illumina [278,502]"	N
6/17/2009	19503088	Gregersen	7-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis"	Rheumatoid arthritis	"2,418 cases, 4,504 controls"	"2,604 cases, 2,882 controls"	8p23.1	BLK	rs2736340-A	rs2736340	0.24	6.00E-09		1.19	[1.13-1.27]	"Illumina [278,502]"	N
6/17/2009	19503088	Gregersen	7-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis"	Rheumatoid arthritis	"2,418 cases, 4,504 controls"	"2,604 cases, 2,882 controls"	1p13.2	PTPN22	rs2476601-?	rs2476601	NR	2.00E-21		NR	NR	"Illumina [278,502]"	N
6/17/2009	19503088	Gregersen	7-Jun-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis"	Rheumatoid arthritis	"2,418 cases, 4,504 controls"	"2,604 cases, 2,882 controls"	9q33.2	"TRAF1, C5"	rs881375-?	rs881375	NR	4.00E-08		NR	NR	"Illumina [278,502]"	N
6/17/2009	19497516	Elmore	6-Jun-09	J Vasc Surg	http://www.ncbi.nlm.nih.gov/pubmed/19497516?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association	Abdominal aortic aneurysm	"123 cases, 112 controls"	"827 cases, 594 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [306,330] (pooled)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	11q13.1	SLC22A12	rs505802-T	rs505802	0.7	2.00E-09		0.06	[0.038-0.074] mg/dl decrease	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	4q22.1	ABCG2	rs2231142-T	rs2231142	0.11	1.00E-10	(women)	0.14	[0.096-0.181] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	1q21.1	PDZK1	rs12129861-A	rs12129861	0.46	3.00E-09		0.06	[0.042-0.083] mg/dl decrease	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	2p23.3	GCKR	rs780094-T	rs780094	0.42	1.00E-09		0.05	[0.035-0.068] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	4p16.1	SLC2A9	rs734553-T	rs734553	0.77	0	(women)	0.4	[0.371-0.423] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	6p22.2	SLC17A1	rs1183201-A	rs1183201	0.48	3.00E-14		0.06	[0.459-0.078] mg/dl decrease	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	6p22.2	"LRRC16A, SCGN"	rs742132-A	rs742132	0.7	9.00E-09		0.05	[0.036-0.072] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	4p16.1	SLC2A9	rs734553-T	rs734553	0.77	1.00E-41	(men)	0.22	[0.188-0.252] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	11q13.1	SLC22A11	rs17300741-A	rs17300741	0.51	7.00E-14		0.06	[0.046-0.078] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	10q21.1	SLC16A9	rs12356193-A	rs12356193	0.83	1.00E-08		0.08	[0.051-0.105] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/22/2009	19503597	Kolz	5-Jun-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations"	Serum uric acid	"12,328 European males, 15,813 European females"	NR	4q22.1	ABCG2	rs2231142-T	rs2231142	0.11	2.00E-18	(men)	0.22	[0.171-0.270] mg/dl increase	"Affymetrix and Illumina [2,493,963] (imputed)"	N
6/16/2009	19488044	Smith	2-Jun-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19488044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of bipolar disorder in European American and African American individuals	Bipolar disorder	"1,001 Caucasian cases, 345 African American cases, 1,033 Caucasian controls, 670 African American controls"	"1,749 Caucasian family members, 1,263 Caucasian cases, 431 Caucasian controls"	19q13.11	DPY19L3	rs2111504-T	rs2111504	0.23	0.000002	(AA)	1.74	[NR]	"Affymetrix [702,044]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	3q27.3	ST6GAL1	rs10937275-?	rs10937275	0.09	1.00E-08	(B*5701 positive)	4.1	[NR]	"Illumina [866,399]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	3q11.2	OR5H2	rs1497546-?	rs1497546	0.02	2.00E-07		6.57	[NR]	"Illumina [866,399]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	12q12	ALG10B	rs6582630-?	rs6582630	0.38	0.000001		2.82	[NR]	"Illumina [866,399]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	9p21.2	C9org82	rs10812428-?	rs10812428	0.31	0.000001		2.85	[NR]	"Illumina [866,399]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	6p21.33	"HCP5, HLA-B"	rs2395029-?	rs2395029	0.05	9.00E-33		45	[19.4-105]	"Illumina [866,399]"	N
6/15/2009	19483685	Daly	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin	Drug-induced liver injury (flucloxacillin)	"58 cases, 282 controls"	NR	15q26.2	MCTP2	rs4984390-?	rs4984390	0.41	0.000004		3.27	[NR]	"Illumina [866,399]"	N
6/14/2009	19483682	Kanetsky	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483682?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer	Testicular cancer	"277 white, non-Hispanic cases, 919 non-Hispanic controls"	"371 non-Hispanic cases + 204 sets of parents, 860 non-Hispanic controls"	12q21.32	KITLG	rs4474514-A	rs4474514	NR	6.00E-15		3.07	[2.29-4.13]	"Affymetrix [611,254]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	12q21.32	KITLG	rs1508595-G	rs995030	0.83	3.00E-30		2.69	[2.10-3.44]	"Illumina [307,666]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	4q24	Intergenic	rs4699052-C	rs4699052	0.61	2.00E-07		1.21	[1.05-1.39]	"Illumina [307,666]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	5q31.3	SPRY4	rs4624820-A	rs4624820	0.54	3.00E-13		1.37	[1.19-1.58]	"Illumina [307,666]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	12q21.32	KITLG	rs995030-G	rs995030	0.8	1.00E-31		2.55	[2.05-3.19]	"Illumina [307,666]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	6p21.31	BAK1	rs210138-G	rs210138	0.2	1.00E-13		1.5	[1.28-1.75]	"Illumina [307,666]"	N
6/14/2009	19483681	Rapley	31-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of testicular germ cell tumor	Testicular germ cell tumor	"730 cases, 1,435 controls"	"571 cases, 1,806 controls"	1q24.1	Intergenic	rs4657482-A	rs4657482	0.33	0.000002		1.14	[0.99-1.31]	"Illumina [307,666]"	N
6/14/2009	19478819	Ng	29-May-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19478819?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.	Nasopharyngeal carcinoma	"111 Chinese cases, 260 Chinese controls"	"168 Chinese cases, 252 Chinese controls"	3p22.2	ITGA9	rs189897-A	rs189897	0.09	7.00E-08		3.18	[1.94-5.21]	"Illumina [533,048]"	N
6/16/2009	19478329	Aston	28-May-09	J Androl	http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia	Male infertility	"52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls"	NR	2q22.1	NXPH2	rs1399645-?	rs1399645	0.02	9.00E-07	(azoospermia)	NR	NR	"Illumina [314,776]"	N
6/16/2009	19478329	Aston	28-May-09	J Androl	http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia	Male infertility	"52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls"	NR	20q13.2	SALL4	rs6068020-?	rs6068020	0.49	5.00E-07	(azoospermia)	NR	NR	"Illumina [314,776]"	N
6/16/2009	19478329	Aston	28-May-09	J Androl	http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia	Male infertility	"52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls"	NR	3q11.2	ARL6	rs9814870-?	rs9814870	0.15	7.00E-07	(oligozoospermia)	NR	NR	"Illumina [314,776]"	N
6/16/2009	19478329	Aston	28-May-09	J Androl	http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia	Male infertility	"52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls"	NR	12p12.2	PDE3A	rs10841496-?	rs10841496	0.58	5.00E-07	(azoospermia)	NR	NR	"Illumina [314,776]"	N
6/16/2009	19478329	Aston	28-May-09	J Androl	http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia	Male infertility	"52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls"	NR	12p13.32	EFCAB4B	rs10848911-?	rs10848911	0.11	0.000004	(azoospermia)	NR	NR	"Illumina [314,776]"	N
6/10/2009	19456320	Ma	28-May-09	Ann Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19456320?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study of autism reveals a common novel risk locus at 5p14.1	Autism	"1,390 family members"	"2,390 family members"	5p14.1	Intergenic	rs10038113-T	rs10038113	0.59	0.000003		1.33	[1.11-1.43]	"Illumina [775,311]"	N
6/14/2009	19465909	Jallow	24-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and fine-resolution association anaylsis of malaria in West Africa	Malaria	"958 Gambian cases, 1,382 Gambian controls, all children"	"1,087 Gambian cases, 2,376 Gambian controls, all children"	7p12.2	DDC	rs1451375-?	rs1451375	0.78	0.000006		1.33	[1.18-1.52]	"Affymetrix [402,814]"	N
6/14/2009	19465909	Jallow	24-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and fine-resolution association anaylsis of malaria in West Africa	Malaria	"958 Gambian cases, 1,382 Gambian controls, all children"	"1,087 Gambian cases, 2,376 Gambian controls, all children"	17p13.1	SCO1	rs6503319-T	rs6503319	0.45	7.00E-07		1.21	[1.12-1.31]	"Affymetrix [402,814]"	N
6/14/2009	19465909	Jallow	24-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and fine-resolution association anaylsis of malaria in West Africa	Malaria	"958 Gambian cases, 1,382 Gambian controls, all children"	"1,087 Gambian cases, 2,376 Gambian controls, all children"	11p15.4	HBB	rs11036238-?	rs11036238	0.14	4.00E-11		1.59	[1.39-1.82]	"Affymetrix [402,814]"	N
6/4/2009	19461586	Norris	21-May-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19461586?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Study and Follow-up Analysis of Adiposity Traits in Hispanic Americans: The IRAS Family Study	Obesity-related traits	229 Hispanic family members	961 Hispanic family members	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [309,200]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	3q26.1	IL12A	rs6441286-G	rs6441286	0.39	2.00E-14		1.54	[1.38-1.72]	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	1p31.3	IL12RB2	rs3790567-A	rs3790567	0.24	3.00E-11		1.51	[1.33-1.70]	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	7q32.1	IRFS-TNPO3	rs10488631-G	rs10488631	NR	2.00E-07		1.52	[1.30-1.78]	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	6p21.3	"c6orf10, BTNL2, HLA-DQB1"	4-SNP haplotype-2	"rs2856683,rs9357152,rs2395148,rs3135363"	0.2	7.00E-10	(CACA)	NR	NR	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	3q26.1	ARF7	rs4679904-G	rs4679904	0.72	0.000001		1.38	[1.21-1.57]	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	6p21.32	"c6orf10, BTNL2, HLA-DQB1"	4-SNP haplotype-1	"rs3135363,rs2395148,rs2856683,rs9357152"	0.01	1.00E-10	(AACA)	NR	NR	"Illumina [305,724]"	N
6/21/2009	19458352	Hirschfield	20-May-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants"	Primary biliary cirrhosis	"505 cases, 1,507 controls"	"up to 526 cases, 1,206 controls"	17q12	IKZF3	rs907092-A	rs907092	0.45	0.000008		1.29	[1.15-1.44]	"Illumina [305,724]"	N
6/14/2009	19454037	Arnett	19-May-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19454037?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study	Left ventricular mass	"101 Caucasian cases, 101 Caucasian controls"	"704 Caucasian siblings, 1,467 African American siblings"	7q21.11	CD36	rs10499859-?	rs10499859	0.45	0.000003	(Caucasian)	0.09	[NR] (LVMI)	"Affymetrix [96,258]"	N
6/14/2009	19454037	Arnett	19-May-09	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19454037?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study	Left ventricular mass	"101 Caucasian cases, 101 Caucasian controls"	"704 Caucasian siblings, 1,467 African American siblings"	5p13.2	RAI14	rs409045-?	rs409045	0.38	8.00E-07	(Caucasian)	0	[NR] (LVMI)	"Affymetrix [96,258]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	18q12.1	B4GALT6	rs10438933-G	rs10438933	0.12	0.000001	(susceptibilty)	1.3	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	21q21.1	NR	rs2823962-?	rs2823962	NR	0.000009	(survival)	NR	NR	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	1p34.2	NT5C1A	rs873917-T	rs873917	0.29	0.000008	(susceptibilty)	1.16	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	2q24.2	RBMS1	rs10192369-T	rs10192369	0.47	0.000009	(susceptibilty)	1.17	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	2p16.1	EFEMP1	rs7577894-T	rs7577894	0.39	0.000001	(site of onset)	1.41	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	2q24.3	SCN7A	rs13015447-T	rs13015447	0.34	0.000007	(site of onset)	1.41	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	5q23.1	SEMA6A	rs7702057-C	rs7702057	0.03	0.000008	(site of onset)	2.05	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	17q24.3	SLC39A11	rs8066857-C	rs8066857	NR	0.000008	(site of onset)	1.48	[NR]	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	6p22.3	ATXN1	rs697739-A	rs697739	NR	0.000004	(age of onset)	2.04	[1.18-2.90] years younger	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	3p26.3	CNTN4	rs2619566-G	rs2619566	NR	0.000007	(age of onset)	3.03	[1.71-4.35] years younger	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	1q24.2	KIFAP3	rs1541160-C	rs1541160	NR	2.00E-08	(survival)	0.58	[0.38-0.78] years older	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	7q36.1	ZNF746	rs855913-A	rs855913	NR	4.00E-08	(survival)	1.08	[0.70-1.46] years older	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	5q23.2	CSNK1G3	rs11241713-T	rs11241713	NR	0.000003	(survival)	0.79	[0.46-1.12] years older	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	1q24.2	SELL	rs3177980-G	rs3177980	NR	0.000004	(survival)	0.51	[0.46-0.56] years older	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	2p22.1	NR	rs3099950-?	rs3099950	NR	0.000008	(survival)	NR	NR	"Illumina [288,357]"	N
6/4/2009	19451621	Landers	18-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"1,821 cases, 2,258 controls"	"538 cases, 556 controls"	1q42.2	DISC1	rs16856202-A	rs16856202	0.04	0.000008	(susceptibilty)	2	[NR]	"Illumina [288,357]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	6q21	LIN28B	rs314277-A	rs314277	0.14	3.00E-13	(age at menarche)	0.16	[0.12-0.20] years older	"Illumina [317,759]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	19q13.42	BRSK1	rs1172822-T	rs1172822	0.37	2.00E-19	(age at natural menopause)	0.49	[0.38-0.60] years younger	"Illumina [317,759]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	20p12.3	"TRMT6, MCM8"	rs16991615-A	rs16991615	0.06	1.00E-21	(age at natural menopause)	1.07	[0.85-1.29] years older	"Illumina [317,759]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	6p24.2	"GCM2, SYCP2L"	rs2153157-T	rs2153157	0.49	5.00E-08	(age at natural menopause)	0.29	[0.19-0.39] years older	"Illumina [317,759]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	5q35.2	UIMC1	rs365132-T	rs365132	0.49	8.00E-14	(age at natural menopause)	0.39	[0.29-0.49] years older	"Illumina [317,759]"	N
6/4/2009	19448621	He	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause	Menarche and menopause (age at onset)	"17,438 Caucasian women"	NR	9q31.2	Intergenic	rs7861820-C	rs7861820	0.48	3.00E-09	(age at menarche)	0.09	[0.06-0.12] years younger	"Illumina [317,759]"	N
6/1/2009	19448623	Ong	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448623?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in LIN28B is associated with the timing of puberty	Menarche (age at onset)	"4,714 women"	"16,373 women"	6q21	LIN28B	rs314276-C	rs314276	0.33	4.00E-16		0.14	[0.11-0.17] years younger	"Affymetrix [up to 390,631]"	N
5/28/2009	19448620	Perry	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448620?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies two loci influencing age at menarche	Menarche (age at onset)	"17,510 women"	NR	6q21	LIN28B	rs7759938-C	rs7759938	0.33	7.00E-09		0.09	[0.05-0.13] years older	Affymetrix & Illumina [~2.5 million] (imputed)	N
5/28/2009	19448620	Perry	17-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448620?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies two loci influencing age at menarche	Menarche (age at onset)	"17,510 women"	NR	9q31.2	"TMEM38B, SLC44A1, FKTN, FSD1L, TAL2, ZNF462"	rs2090409-A	rs2090409	0.31	2.00E-09		0.1	[0.06-0.14] years younger	Affymetrix & Illumina [~2.5 million] (imputed)	N
6/1/2009	19448189	Perlis	15-May-09	Am J Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19448189?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder	Response to lithium treatment in bipolar disorder	"458 lithium-treated subjects, 719 non-lithium treated subjects"	359 subjects	NR	NR	NR		NR	NS	NS	NR	NR	Affymetrix [~1.4 million] (imputed)	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	20p12.3	MCM8	rs236114-A	rs236114	0.21	1.00E-10		0.5	[0.34-0.65] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	19q13.42	"BRSK1, TMEM224, SUV420H2"	rs1172822-T	rs1172822	0.39	6.00E-11		0.39	[0.27-0.51] years younger	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	13q34	"LOC121793, ARHGEF7"	rs7333181-A	rs7333181	0.12	3.00E-08		0.52	[0.34-0.70] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	11q25	NR	rs4397868-?	rs4397868	NR	3.00E-07		0.4	[0.25-0.55] years younger	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	7q22.3	NR	rs17153527-?	rs17153527	NR	4.00E-07		0.51	[0.31-0.71] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	20p12.3	NR	rs2326679-?	rs2326679	NR	0.000002		0.32	[0.19-0.45] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	16q24.2	NR	rs4843747-?	rs4843747	NR	2.00E-07		0.39	[0.24-0.54] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	8p12	NR	rs6468442-?	rs6468442	NR	3.00E-07		0.39	[0.24-0.54] years younger	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	2q23.3	NR	rs11889862-?	rs11889862	NR	0.000002		0.36	[0.21-0.51] years younger	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	6p21.32	NR	rs494620-?	rs494620	NR	5.00E-07		0.3	[0.18-0.42] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	9q21.31	NR	rs2151145-?	rs2151145	NR	1.00E-07		0.41	[0.26-0.56] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	3q26.2	NR	rs4955755-?	rs4955755	NR	7.00E-07		0.34	[0.21-0.47] years older	"Illumina [315,418]"	N
5/28/2009	19448619	Stolk	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Loci at chromosomes 13, 19 and 20 influence age at natural menopause."	Menopause (age at onset)	"2,979 women"	"2,560 women"	14q32.31	NR	rs4906172-?	rs4906172	NR	0.000003		0.36	[0.21-0.51] years younger	"Illumina [315,418]"	N
6/1/2009	19448622	Sulem	15-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19448622?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche	Menarche (age at onset)	"15,297 Icelandic women"	"10,040 Icelandic women"	6q21	"LIN28B, HACE1, E3 ubiquitin protein ligase 1, BVES, POPDC3"	rs314280-T	rs314280	0.48	2.00E-14		1.2	[0.9-1.5] months older	"Illumina [304,226]"	N
5/26/2009	19442274	Fei	14-May-09	Arthritis Res Ther	http://www.ncbi.nlm.nih.gov/pubmed/19442274?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of novel genetic susceptibility loci for Behcet's disease using a genome-wide association study	Behcet's disease	"152 cases, 170 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~500,000] (pooled)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	6p21.32	MHC	rs9268645-?	rs9268645	NR	1.00E-100		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	7p15.2	Intergenic	rs7804356-?	rs7804356	0.76	5.00E-09		1.14	[1.06-1.22]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	17p13.1	Intergenic	rs16956936-?	rs16956936	0.86	5.00E-07		1.09	[1.00-1.19]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	1p13.2	PTPN22	rs2476601-?	rs2476601	NR	9.00E-85		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	2q24.2	IFIH1	rs1990760-?	rs1990760	NR	7.00E-09		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	2q33.2	CTLA4	rs3087243-?	rs3087243	NR	1.00E-15		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	4q27	IL2	rs4505848-?	rs4505848	NR	5.00E-13		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	6q15	BACH2	rs11755527-?	rs11755527	NR	5.00E-08		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	10p15.1	IL2RA	rs12251307-?	rs12251307	NR	1.00E-13		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	10p15.1	PRKCQ	rs11258747-?	rs11258747	NR	1.00E-07		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	11p15.5	INS	rs7111341-?	rs7111341	NR	4.00E-48		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	12q13.2	ERBB3	rs2292239-?	rs2292239	NR	2.00E-25		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	12q24.12	SH2B3	rs3184504-?	rs3184504	NR	3.00E-27		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	15q25.1	CTSH	rs3825932-?	rs3825932	NR	8.00E-08		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	16p13.13	CLEC16A	rs12708716-?	rs12708716	NR	2.00E-16		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	18p11.21	PTPN2	rs1893217-?	rs1893217	NR	4.00E-15		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	21q22.3	UBASH3A	rs11203203-?	rs11203203	NR	2.00E-09		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	22q13.1	C1QTNF6	rs229541-?	rs229541	NR	2.00E-07		NR	NR	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	1q32.1	IL10	rs3024505-?	rs3024505	0.83	2.00E-09		1.19	[1.10-1.30]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	4p15.2	Intergenic	rs10517086-A	rs10517086	0.3	5.00E-10		1.09	[1.02-1.17]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	6q22.32	C6orf173	rs9388489-G	rs9388489	0.45	4.00E-13		1.17	[1.10-1.24]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	7p12.1	COBL	rs4948088-?	rs4948088	0.95	4.00E-08		1.3	[1.11-1.49]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	9p24.2	GLIS3	rs7020673-?	rs7020673	0.5	5.00E-12		1.14	[1.08-1.20]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	10q23.31	C10orf59	rs10509540-?	rs10509540	0.71	1.00E-28		1.33	[1.25-1.43]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	12p13.31	CD69	rs4763879-A	rs4763879	0.37	2.00E-11		1.09	[1.02-1.16]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	14q24.1	Intergenic	rs1465788-?	rs1465788	0.71	2.00E-12		1.16	[1.10-1.25]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	14q32.2	Intergenic	rs4900384-G	rs4900384	0.29	4.00E-09		1.09	[1.02-1.16]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	16p11.2	IL27	rs4788084-G	rs4788084	0.42	3.00E-13		1.09	[1.02-1.16]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	16q23.1	Intergenic	rs7202877-G	rs7202877	0.1	3.00E-15		1.28	[1.17-1.41]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	17q12	ORMDL3	rs2290400-?	rs2290400	0.5	6.00E-13		1.15	[1.08-1.22]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	17q21.2	Intergenic	rs7221109-?	rs7221109	0.65	1.00E-09		1.05	[0.99-1.12]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	19q13.32	Intergenic	rs425105-?	rs425105	0.84	3.00E-11		1.16	[1.08-1.27]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	20p13	Intergenic	rs2281808-?	rs2281808	0.64	1.00E-11		1.11	[1.05-1.19]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	22q12.2	Intergenic	rs5753037-T	rs5753037	0.39	3.00E-16		1.1	[1.04-1.17]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	Xq28	Intergenic	rs2664170-G	rs2664170	0.32	8.00E-09		1.16	[1.07-1.24]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	1p31.3	PGM1	rs2269241-G	rs2269241	0.19	4.00E-07		1.1	[1.02-1.18]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	2p25.1	Intergenic	rs1534422-G	rs1534422	0.46	0.000002		1.08	[1.02-1.15]	"Affymetrix & Illumina [841,622] (imputed)"	N
6/1/2009	19430480	Barrett	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes	Type 1 diabetes	"7,514 cases, 9,045 controls"	"4,267 cases, 4,670 controls, 4,342 trios"	16p12.3	Intergenic	rs12444268-A	rs12444268	0.3	2.00E-07		1.1	[1.03-1.17]	"Affymetrix & Illumina [841,622] (imputed)"	N
5/27/2009	19430482	Kottgen	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Multiple loci associated with indices of renal function and chronic kidney disease	Renal function and chronic kidney disease	"19,877 individuals, up to 2,388 cases"	"21,466 individuals, up to 1,932 cases"	16p12.3	UMOD	rs12917707-T	rs12917707	0.18	5.00E-16	(eGFRcrea)	0.02	[0.014-0.022] ml/min/1.73m2 increase	Affymetrix & Illumina [~2.5 million] (imputed)	N
5/27/2009	19430482	Kottgen	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Multiple loci associated with indices of renal function and chronic kidney disease	Renal function and chronic kidney disease	"19,877 individuals, up to 2,388 cases"	"21,466 individuals, up to 1,932 cases"	16p12.3	UMOD	rs12917707-G	rs12917707	0.18	2.00E-12	(CKD)	1.25	[1.18-1.33]	Affymetrix & Illumina [~2.5 million] (imputed)	N
5/27/2009	19430482	Kottgen	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Multiple loci associated with indices of renal function and chronic kidney disease	Renal function and chronic kidney disease	"19,877 individuals, up to 2,388 cases"	"21,466 individuals, up to 1,932 cases"	4q21.1	SHROOM3	rs17319721-A	rs17319721	0.44	1.00E-12	(eGFRcrea)	0.01	[0.008-0.016] ml/min/1.73m2 decrease	Affymetrix & Illumina [~2.5 million] (imputed)	N
5/27/2009	19430482	Kottgen	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Multiple loci associated with indices of renal function and chronic kidney disease	Renal function and chronic kidney disease	"19,877 individuals, up to 2,388 cases"	"21,466 individuals, up to 1,932 cases"	15q21.1	"SPATA5L1, GATM"	rs2467853-G	rs2467853	0.38	6.00E-14	(eGFRcrea)	0.01	[0.009-0.017] ml/min/1.73m2 decrease	Affymetrix & Illumina [~2.5 million] (imputed)	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	12q21.33	ATP2B1	rs2681472-A	rs2681472	0.83	1.00E-09		0.5	[0.34-0.66] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	15q24.1	"CSK, ULK3"	rs6495122-A	rs6495122	0.42	2.00E-10		0.4	[0.28-0.52] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	11p15.1	PLEKHA7	rs11024074-T	rs11024074	0.72	0.000001		0.33	[0.19-0.47] mm Hg decrease	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	10p12.33	CACNB2	rs11014166-A	rs11014166	0.66	1.00E-08		0.37	[0.25-0.49] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	12q24.21	"TBX3, TBX5"	rs2384550-A	rs2384550	0.35	4.00E-08		0.35	[0.23-0.47] mm Hg decrease	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	12q24.12	SH2B3	rs3184504-T	rs3184504	0.48	3.00E-14		0.48	[0.36-0.60] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Diastolic blood pressure	"29,136 individuals"	"34,433 individuals"	3p22.1	ULK4	rs9815354-A	rs9815354	0.17	3.00E-09		0.49	[0.33-0.65] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Hypertension	"29,136 individuals"	"34,433 individuals"	10p12.33	CACNB2	rs11014166-A	rs11014166	0.66	6.00E-08		0.09	[0.05-0.13] increase in log odds	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Hypertension	"29,136 individuals"	"34,433 individuals"	20q13.32	"ZNF831, EDN3"	rs16982520-A	rs16982520	0.88	2.00E-07		0.13	[0.09-0.17] decrease in log odds	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Hypertension	"29,136 individuals"	"34,433 individuals"	12q21.33	ATP2B1	rs2681472-A	rs2681472	0.83	2.00E-11		0.15	[0.11-0.19] increase in log odds	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Hypertension	"29,136 individuals"	"34,433 individuals"	8p23.1	MSRA	rs11775334-A	rs11775334	0.32	0.000004		0.08	[0.04-0.12] increase in log odds	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	3q26.2	MDS1	rs448378-A	rs448378	0.52	1.00E-07		0.51	[0.31-0.71] mm Hg decrease	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	10p12.33	CACNB2	rs11014166-A	rs11014166	0.66	7.00E-07		0.5	[0.30-0.70] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	12q24.12	SH2B3	rs3184504-T	rs3184504	0.48	5.00E-09		0.58	[0.38-0.78] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	10q24.32	CYP17A1	rs1004467-A	rs1004467	0.9	1.00E-10		1.05	[0.74-1.36] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	12q21.33	ATP2B1	rs2681492-T	rs2681492	0.8	4.00E-11		0.85	[0.60-1.10] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	11p15.1	PLEKHA7	rs381815-T	rs381815	0.26	2.00E-09		0.65	[0.43-0.87] mm Hg increase	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430479	Levy	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of blood pressure and hypertension	Systolic blood pressure	"29,136 individuals"	"34,433 individuals"	1p36.22	CASZ1	rs12046278-T	rs12046278	0.64	0.000005		0.53	[0.29-0.77] mm Hg decrease	"Affymetrix & Illumina [2,533,153](imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	4q21.21	"FGF5, PRDM8, c4orf22"	rs16998073-T	rs16998073	0.21	1.00E-21		0.5	[0.40-0.60] mm Hg increase	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	3q26.2	MDS1	rs1918974-T	rs1918974	0.54	8.00E-08		0.27	[0.17-0.37] mm Hg decrease	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	17q21.32	"ZNF652, PHB"	rs16948048-G	rs16948048	0.39	5.00E-09		0.31	[0.21-0.41] mm Hg increase	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	12q24.12	"ATXN2, SH2B3"	rs653178-T	rs653178	0.53	3.00E-18		0.46	[0.36-0.56] mm Hg decrease	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	15q24.1	"CYP1A1, CYP1A2, CSK, LMAN1L, CPLX3, ARID3B"	rs1378942-C	rs1378942	0.36	1.00E-23		0.43	[0.35-0.51] mm Hg increase	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Diastolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	10q21.2	"c10orf107, TMEM26, RTKN2, RHOBTB1, ARID5B"	rs1530440-T	rs1530440	0.19	1.00E-09		0.39	[0.27-0.51] mm Hg decrease	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Systolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	17q21.31	"PLCD3, ACBD4, HEXIM1, HEXIM2"	rs12946454-T	rs12946454	0.28	1.00E-08		0.57	[0.37-0.77] mm Hg increase	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Systolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	1p36.22	"MTHFR, NPPA, CLCN6, NPPB, AGTRAP"	rs17367504-G	rs17367504	0.14	2.00E-13		0.85	[0.63-1.07] mm Hg decrease	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/19/2009	19430483	Newton-Cheh	10-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies eight loci associated with blood pressure	Systolic blood pressure	"34,433 individuals"	"Up to 100,347 white individuals, up to 12,889 Indian Asian individuals"	10q24.32	"CYP17A1, AS3MT, CNNM2, NT5C2"	rs11191548-T	rs11191548	0.91	7.00E-24		1.16	[0.92-1.40] mm Hg increase	"Affymetrix & Illumina [2,497,993] (imputed)"	N
5/21/2009	19430760	Rich	9-May-09	Diabetologia	http://www.ncbi.nlm.nih.gov/pubmed/19430760?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).	Insulin response	229 family members	961 family members	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [309,200]"	N
5/20/2009	19426955	Himes	7-May-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19426955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene	Asthma	"422 cases, 1,533 controls"	"3,750 white cases, 13,365 white controls, 592 white trios, 1,903 black cases, 2,432 black controls, 929 black family members"	5q12.1	PDE4D	rs1588265-C	rs1588265	0.29	3.00E-08		1.18	[1.08-1.30]	"Illumina [518,230]"	N
5/21/2009	19421330	Yang	7-May-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19421330?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan	Hypertension (young onset)	"175 Han Chinese cases, 175 Han Chinese controls"	"833 Han Chinese cases, 833 Han Chinese controls"	2p22.3	"LOC344371, MYADML, FAM98A, RASGRP3"	4-SNP-haplotype	"rs6729869,rs10495809,rs9308945,rs6711736"	NR	3.00E-10		NR	NR	"Affymetrix [91,713]"	N
5/19/2009	19419973	Sanna	6-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia	Bilirubin levels	"4,300 individuals"	"2,692 individuals"	12p12.2	SLC01B3	rs2117032-C	rs2117032	0.47	3.00E-14		0.13	[0.08-0.18] SD increase	"Affymetrix [362,129]"	N
5/19/2009	19419973	Sanna	6-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia	Bilirubin levels	"4,300 individuals"	"2,692 individuals"	Xq28	G6PD	rs766420-G	rs766420	0.18	9.00E-09		0.18	[0.12-0.24] SD decrease	"Affymetrix [362,129]"	N
5/19/2009	19419973	Sanna	6-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia	Bilirubin levels	"4,300 individuals"	"2,692 individuals"	2q37.1	UGT1A1	rs887829-T	rs887829	0.3	1.00E-69		0.57	[0.50-0.63] SD decrease	"Affymetrix [362,129]"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	8p12	NR	rs6990255-T	rs6990255	0.95	0.000006		1.33	[1.18-1.51]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	9q34.13	NR	rs2905072-A	rs2905072	0.77	0.000006		1.21	[1.11-1.32]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	11q13.1	NR	rs2242663-T	rs2242663	0.25	0.000001		1.2	[1.11-1.29]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	17q21.33	NR	rs1035050-T	rs1035050	0.4	0.000009		1.17	[1.09-1.25]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	19p13.3	NR	rs7250872-T	rs7250872	0.69	0.000002		1.21	[1.12-1.31]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	15q23	NR	rs6494849-A	rs6494849	0.12	0.000007		1.23	[1.13-1.35]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	3p21.1	"ITIH1, NEK4"	rs1042779-A	rs1042779	0.63	2.00E-07		1.19	[1.11-1.27]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	4q12	KIT	rs2537859-T	rs2537859	0.6	0.000004		1.16	[1.09-1.24]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	5q15	MCTP1	rs17418283-C	rs17418283	0.28	1.00E-07		1.21	[1.13-1.30]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	1p32.1	NF1A	rs472913-C	rs472913	0.5	2.00E-07		1.18	[1.11-1.25]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	2p12	CTNNA2	rs13409348-G	rs13409348	0.24	0.000003		1.2	[1.11-1.29]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	2q11.2	Intergenic	rs6733011-G	rs6733011	0.46	0.000003		1.17	[1.10-1.25]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/14/2009	19416921	Scott	5-May-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry	Bipolar disorder	"3,683 cases, 14,507 controls"	NR	3q26.1	NR	rs7427021-G	rs7427021	0.56	0.000005		1.16	[1.09-1.24]	"Affymetrix and Illumina [2,366,197] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	2p11.2	KRCC1	rs12714207-T	rs12714207	0.03	5.00E-07		0.03	[0.01-0.05] umol/l decrease in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	2q37.1	UGT1A1	rs6742078-T	rs6742078	0.32	0		0.23	[0.21-0.25] umol/l increase in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	11p15.4	SLC22A18	rs16928809-A	rs16928809	0.09	1.00E-07		0.06	[0.04-0.08] umol/l increase in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	12p12.1	"SLCO1B1,LST-3TM12,SLCO1A2"	rs4149056-C	rs4149056	0.15	7.00E-13		0.05	[0.03-0.07] umol/l increase in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	4q28.1	Intergenic	rs1986655-A	rs1986655	0.17	0.000002		0.02	[0.00-0.04] umol/l decrease in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	7q21.11	SEMA3C	rs4236644-A	rs4236644	0.26	0.000002		0.02	[0.00-0.04] umol/l decrease in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	13q34	ARHGEF7	rs4773330-A	rs4773330	0.12	0.000008		0.04	[0.02-0.06] umol/l decrease in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/12/2009	19414484	Johnson	4-May-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association meta-analysis for total serum bilirubin levels	Serum bilirubin levels	"9,264 individuals"	NR	6p22.1	HIST1H2BC	rs12206204-T	rs12206204	0.02	8.00E-07		0.18	[0.10-0.26] umol/l increase in log(tbil)	"Affymetrix & Illumina [2,555,103] (imputed)"	N
5/7/2009	19412175	Capasso	3-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19412175?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in BARD1 influence susceptibility to high-risk neuroblastoma	Neuroblastoma (high-risk)	"397 cases, 2,043 controls"	"189 cases, 1,178 controls"	2q35	BARD1	rs6435862-G	rs6435862	0.29	9.00E-18		1.68	[1.49-1.90]	"Illumina [462,866]"	N
5/7/2009	19412176	Hallmayer	3-May-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19412176?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Narcolepsy is strongly associated with the T-cell receptor alpha locus	Narcolepsy	"807 Caucasian cases, 1,074 Caucasian controls"	"363 Caucasian cases, 355 Caucasian controls, 561 Asian cases, 605 Asian controls, 133 African American cases, 144 African American controls"	14q11.2	"TRA-alpha, TRAJ10"	rs1154155-C	rs1154155	0.14	3.00E-22		1.69	[1.52-1.88]	"Affymetrix [549,596]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	11p15.5	KCNQ1	rs2237892-C	rs2237892	0.59	1.00E-26		1.33	[1.27-1.41]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	3q27.2	IGF2BP2	rs4402960-T	rs4402960	0.31	0.000001		1.14	[1.08-1.21]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.57	2.00E-14		1.22	[1.16-1.28]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	9p21.3	"CDKN2A, CDKN2B"	rs2383208-A	rs2383208	0.55	2.00E-29		1.34	[1.27-1.41]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	10q22.33	HHEX	rs1111875-C	rs1111875	0.28	7.00E-12		1.21	[1.15-1.28]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	10q25.2	TCF7L2	rs7903146-T	rs7903146	0.04	8.00E-12		1.54	[1.36-1.74]	"Illumina [482,625]"	N
5/7/2009	19401414	Takeuchi	29-Apr-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population	Type 2 diabetes	"519 Japanese cases, 503 Japanese controls"	"5,629 Japanese cases, 7,370 Japanese controls"	6p22.3	CDKAL1	rs4712523-G	rs4712523	0.41	7.00E-20		1.27	[1.21-1.33]	"Illumina [482,625]"	N
5/11/2009	19404256	Wang	28-Apr-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19404256?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common genetic variants on 5p14.1 associate with autism spectrum disorders	Autism	"3,101 family members, 1,204 cases, 6,491 controls"	"1,390 family members, 108 cases, 540 controls"	5p14.1	"CDH10,CDH9"	rs4307059-T	rs4307059	0.61	2.00E-10		1.19	[NR]	"Illumina [474,019]"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	16q12.2	FTO	rs9939609-A	rs9939609	0.13	2.00E-07	(BMI)	0.24	[0.14-0.32] kg/m2 increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	7q31.31	FAM3C	rs7776725-C	rs7776725	0.13	1.00E-11	(BD-RT)	NR	NR	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	7q31.31	FAM3C	rs7776725-C	rs7776725	0.13	0.000002	(BD-TT)	NR	NR	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	6q22.31	LOC644502	rs12110693-A	rs12110693	0.49	2.00E-09	(pulse rate)	0.66	[0.45-0.87] beats per minute increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	12q21.33	ATP2B1	rs17249754-A	rs17249754	0.37	0.000003	(DBP)	0.63	[0.37-0.89] mm Hg decrease	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	12q21.33	ATP2B1	rs17249754-A	rs17249754	0.37	1.00E-07	(SBP)	1.06	[0.67-1.45] mm Hg decrease	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	1q32.2	"CD46, LOC148696"	rs12731740-T	rs12731740	0.1	3.00E-09	(pulse rate)	1.09	[0.72-1.44] beats per minute increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Biomedical quantitative traits	"8,842 Korean individuals"	"7,861 Korean individuals"	12q24.13	C12orf51	rs2074356-T	rs2074356	0.15	8.00E-12	(waist-hip ratio)	0.01	[0.004-0.008] decrease	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Height	"8,842 Korean individuals"	"7,861 Korean individuals"	1p12	Intergenic	rs17038182-C	rs17038182	0.42	5.00E-07		0.3	[0.18-0.42] cm decrease	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Height	"8,842 Korean individuals"	"7,861 Korean individuals"	3q23	ZBTB38	rs10513137-A	rs10513137	0.26	6.00E-12		0.46	[0.33-0.59] cm increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Height	"8,842 Korean individuals"	"7,861 Korean individuals"	2p16.1	EFEMP1	rs3791675-G	rs3791675	0.22	2.00E-09		0.42	[0.28-0.56] cm increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Height	"8,842 Korean individuals"	"7,861 Korean individuals"	6p21.31	HMGA1	rs6918981-G	rs6918981	0.21	3.00E-08		0.4	[0.26-0.54] cm increase	"Affymetrix [2,156,535] (imputed)"	N
5/5/2009	19396169	Cho	26-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits	Height	"8,842 Korean individuals"	"7,861 Korean individuals"	8q12.1	PLAG1	rs13273123-G	rs13273123	0.07	1.00E-09		0.71	[0.48-0.94] cm decrease	"Affymetrix [2,156,535] (imputed)"	N
4/23/2009	19369658	Ikram	15-Apr-09	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/19369658?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Studies of Stroke	Stroke	"19,602 Caucasian individuals"	"3,004 African American individuals, 652 Caucasian cases, 3,613 Caucasian controls"	12p13.33	NINJ2	rs12425791-A	rs12425791	0.19	1.00E-09	(ischemic stroke)	1.29	[1.19-1.41]	"Affymetrix & Illumina [2,194,468]"	N
4/22/2009	19367585	Poduslo	14-Apr-09	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/19367585?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis	Aging	"89 cases, 227 controls"	NR	2q22.1	LRP1B	rs12474609-?	rs12474609	NR	6.00E-09		NR	NR	"Affymetrix [469,218]"	N
5/5/2009	19359809	Hiura	10-Apr-09	Circ J	http://www.ncbi.nlm.nih.gov/pubmed/19359809?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of Genetic Markers Associated With High-Density Lipoprotein-Cholesterol by Genome-Wide Screening in a Japanese Population	LDL cholesterol	900 Japanese individuals	"1,810 Japanese individuals"	16q13	CETP	rs3764261-A	rs3764261	0.2	3.00E-12		6.2	mg/dl increase	"Illumina [368,274]"	N
4/22/2009	19359265	Mangino	8-Apr-09	J Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/19359265?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length	Telomere length	"1,625 women"	"1,165 individuals"	18q12.2	"BRUNOL4, VPS34"	rs2162440-G	rs2162440	NR	0.000003		106	[62.88-149.12] base pairs shorter	"Illumina [~314,075]"	N
4/14/2009	19349984	Esparza-Gordillo	6-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19349984?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A common variant on chromosome 11q13 is associated with atopic dermatitis	Atopic dermatitis	"939 cases, 975 controls, 1,097 family members"	"2,637 cases, 3,957 controls"	11q13.5	C11orf30	rs7927894-A	rs7927894	0.36	8.00E-10		1.22	[1.15-1.30]	"Affymetrix [342,303]"	N
4/16/2009	19349983	Kamatani	6-Apr-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19349983?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians	Hepatitis B	"179 Japanese cases, 934 Japanese controls"	"1,599 Japanese cases, 2,821 Japanese controls, 308 Thai cases, 546 Thai controls"	6p21.32	HLA-DPB1	rs9277535-G	rs9277535	0.56	6.00E-39		1.75	[1.61-1.92]	"Illumina [499,544]"	N
5/11/2009	19403135	Yamada	5-Apr-09	Atherosclerosis	http://www.ncbi.nlm.nih.gov/pubmed/19403135?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study	Ischemic stroke	"131 cases, 135 controls"	"776 cases, 5,205 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~520,000]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	4q31.22	HHIP	rs1812175-?	rs1812175	0.49	0.000004		0.06	[0.03-0.09] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	14q24.3	TMED10	rs910316-?	rs910316	0.15	1.00E-07		0.05	[0.03-0.07] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	13q14.3	DLEU7	rs3118914-?	rs3118914	0.39	4.00E-10		0.08	[0.05-0.11] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	7p22.2	GNA12	rs1182188-?	rs1182188	0.27	3.00E-09		0.07	[0.04-0.10] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	6q24.1	GPR126	rs6570507-?	rs6570507	0.42	4.00E-11		0.08	[0.06-0.10] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	6p21.33	HLA-B	rs13437082-?	rs13437082	0.13	5.00E-08		0.07	[0.04-0.10] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	1p36.11	CATSPER4	rs11809207-?	rs11809207	0.23	6.00E-08		0.07	[0.04-0.10] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	4p15.32	LCORL	rs6830062-?	rs6830062	0.23	5.00E-09		0.1	[0.07-0.13] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	7q21.2	CDK6	rs2282978-?	rs2282978	0.08	1.00E-08		0.06	[0.04-0.08] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	9p13.3	WDR40A	rs7871764-?	rs7871764	0.44	0.000002		0.06	[0.03-0.09] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	8q12.1	PLAG1	rs7815788-?	rs7815788	0.39	0.000005		0.07	[0.04-0.10] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	20q11.22	UQCC	rs6088813-?	rs6088813	0.11	1.00E-13		0.09	[0.07-0.11] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	15q25.2	ADAMTSL3	rs4842838-?	rs4842838	0.32	3.00E-08		0.06	[0.04-0.07] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	12q14.3	HMGA2	rs8756-?	rs8756	0.17	5.00E-14		0.08	[0.06-0.10] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	7p15.1	JAZF1	rs849141-?	rs849141	0.23	3.00E-11		0.08	[0.06-0.10] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	6p21.31	"HMGA1,C6orf106"	rs1776897-?	rs1776897	0.49	8.00E-11		0.12	[0.08-0.16] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	6p22.1	HIST1H1D	rs10946808-?	rs10946808	0.43	6.00E-12		0.07	[0.04-0.10] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	5p13.3	NPR3	rs10472828-?	rs10472828	0.26	3.00E-07		0.06	[0.04-0.08] SD decrease	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	3q23	ZBTB38	rs6763931-?	rs6763931	0.35	3.00E-12		0.07	[0.05-0.09] SD increase	"Illumina [229,216]"	N
4/22/2009	19343178	Soranzo	3-Apr-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size	Height	"12,611 individuals"	"7,187 individuals"	4q21.21	PRKG2	rs710841-?	rs710841	0.12	2.00E-08		0.07	[0.04-0.10] SD increase	"Illumina [229,216]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	14q32.2	Intergenic	rs17094273-A	rs17094273	NR	9.00E-08		0.2	[0.12-0.28] increase in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	5p13.3	MATP	rs35391-T	rs35391	NR	3.00E-10		0.44	[0.30-0.58] decrease in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	5q33.1	PPARGC1B	rs32579-A	rs32579	NR	0.000004		0.11	[0.07-0.15] decrease in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	12q13.13	LOC440100	rs7969151-A	rs7969151	0.21	0.000002		0.13	[0.07-0.19] increase in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	11q14.3	TYR	rs1393350-A	rs1393350	NR	2.00E-13		0.19	[0.13-0.25] increase in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	6p25.3	EXOC2	rs12210050-T	rs12210050	NR	5.00E-14		0.22	[0.16-0.28] increase in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	21q22.3	PRDM15	rs7279297-G	rs7279297	NR	0.000003		0.12	[0.06-0.18] decrease in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	16q24.3	MC1R	rs154659-C	rs154659	NR	7.00E-08		0.14	[0.08-0.20] increase in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	11q14.3	GRM5	rs10831496-G	rs10831496	NR	5.00E-09		0.14	[0.10-0.18] decrease in tanning ability score	"Illumina [528,173]"	N
4/13/2009	19340012	Nan	2-Apr-09	J Invest Dermatol	http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry	Tanning	"2,287 women"	870 controls	16q24.3	MC1R	rs11648785-T	rs11648785	NR	3.00E-09		0.14	[0.10-0.18] decrease in tanning ability score	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	2q35	Intergenic	rs13387042-A	rs13387042	0.51	2.00E-08		1.25	[1.15-1.37]	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	5q11.2	MAP3K1	rs16886165-G	rs16886165	0.15	5.00E-07		1.23	[1.12-1.35]	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	14q24.1	RAD51L1	rs999737-C	rs999737	0.76	2.00E-07		1.06	[1.01-1.14]	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	1p11.2	Intergenic	rs11249433-C	rs11249433	0.39	7.00E-10		1.16	[1.09-1.24]	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	10q26.13	FGFR2	rs2981579-T	rs2981579	0.41	2.00E-10		1.17	[1.07-1.27]	"Illumina [528,173]"	N
4/3/2009	19330030	Thomas	29-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)	Breast cancer	"1,145 cases, 1,142 controls"	"8,625 cases, 9,657 controls"	16q12.1	TOX3	rs3803662-T	rs3803662	0.27	1.00E-09		1.16	[1.07-1.27]	"Illumina [528,173]"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	3p22.2	SCN5A	rs12053903-C	rs12053903	0.34	1.00E-14		1.23	[0.88-1.57] msec decrease	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	1q23.3	NOS1AP	rs12029454-A	rs12029454	0.15	3.00E-45		2.98	[2.63-3.32] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	17q12	"LIG3,RFFL"	rs2074518-T	rs2074518	0.46	6.00E-12		1.05	[0.71-1.39] msec decrease	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	1q23.3	NOS1AP	rs16857031-G	rs16857031	0.14	1.00E-34		2.63	[2.28-2.97] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	7q36.1	KCNH2	rs2968864-C	rs2968864	0.25	8.00E-16		1.4	[1.06-1.74] msec decrease	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	7q36.1	KCNH2	rs4725982-T	rs4725982	0.22	5.00E-16		1.58	[1.23-1.92] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	1p36.31	"RNF207,NPHP4, CHDS, ACOT7, PLEKHG5, KLH21"	rs846111-C	rs846111	0.28	1.00E-16		1.75	[1.41-2.09] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	11p15.5	KCNQ1	rs12576239-T	rs12576239	0.13	1.00E-15		1.75	[1.41-2.09] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	6q22.31	"c6orf204,SLC35F1, PLN, ASF1A"	rs11756438-A	rs11756438	0.47	5.00E-22		1.4	[1.06-1.74] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	16q21	"CNOT1,GINS3, NDRG4, SLC38A7, GOT2"	rs37062-G	rs37062	0.24	3.00E-25		1.75	[1.41-2.09] msec decrease	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	11p15.5	KCNQ1	rs2074238-T	rs2074238	0.06	3.00E-17		7.88	[6.16-9.59] msec decrease	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	1q23.3	NOS1AP	rs12143842-T	rs12143842	0.26	2.00E-78		3.15	[2.81-3.49] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
3/31/2009	19305408	Newton-Cheh	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci influence QT interval duation in the QTGEN Study	QT interval	"13,685 individuals"	"15,854 individuals"	16p13.13	"LITAF,CLEC16A, SNN, ZC3H7A, TNFRSF17"	rs8049607-T	rs8049607	0.49	5.00E-15		1.23	[0.88-1.57] msec increase	"Affymetrix and Illumina [up to 2,543,686] (imputed)"	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	1q23.3	NOS1AP	rs4657178-T	rs4657178	0.33	7.00E-33		2.19	[1.76-2.62] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	1q24.2	ATP1B1	rs10919071-A	rs10919071	0.87	1.00E-15		2.05	[1.48-2.62] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	1p36.31	RNF207	rs846111-C	rs846111	0.29	4.00E-16		1.49	[1.00-1.98] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	11p15.5	KCNQ1	rs12296050-T	rs12296050	0.2	3.00E-17		1.44	[0.95-1.93] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	16p13.13	LITAF	rs8049607-T	rs8049607	0.46	6.00E-15		1.25	[0.81-1.69] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	17q24.3	KCNJ2	rs17779747-T	rs17779747	0.35	6.00E-12		1.02	[0.53-1.51] ms decrease	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	16q21	NDRG4	rs7188697-A	rs7188697	0.74	7.00E-25		1.66	[1.20-2.12] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	7q36.1	KCNH2	rs2968863-T	rs2968863	0.29	2.00E-15		1.35	[0.90-1.80] ms decrease	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	6q22.31	PLN	rs11970286-T	rs11970286	0.44	2.00E-24		1.64	[1.25-2.03] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	6q22.31	PLN	rs12210810-C	rs12210810	0.06	2.00E-17		3.13	[2.29-3.97] ms decrease	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	1q23.3	NOS1AP	rs12143842-T	rs12143842	0.24	2.00E-78		2.88	[2.43-3.33] ms increase	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19305409	Pfeufer	22-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at ten loci modulate the QT interval duration in the QTSCD Study	QT interval	"15,842 individuals"	"up to 13,602 individuals"	3p22.2	SCN5A	rs11129795-A	rs11129795	0.23	5.00E-14		1.27	[0.82-1.72] ms decrease	Affymetrix and Illumina [unsure] (imputed)	N
4/2/2009	19304780	Org	20-Mar-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19304780?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations	Hypertension	"364 cases, 590 controls"	"1,043 cases, 1,769 controls"	16q23.3	CDH13	rs11646213-T	rs11646213	0.6	0.000008		1.28	[1.15-1.43]	"Affymetrix [395,912]"	N
3/31/2009	19300482	Pillai	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci	Chronic Obstructive Pulmonary Disease	"823 cases, 810 controls"	"2,840 family members, 389 cases, 472 controls"	15q25.1	"CHRNA3,CHRNA4,CHRNA5, IREB2, PSMA4, NP_001013641.2,Q9UD29"	rs8034191-C	rs8034191	0.33	1.00E-10		1.4	[1.18-1.67]	"Ilumina [493,609]"	N
3/31/2009	19300482	Pillai	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci	Chronic Obstructive Pulmonary Disease	"823 cases, 810 controls"	"2,840 family members, 389 cases, 472 controls"	4q31.22	HHIP	rs1828591-?	rs1828591	NR	1.00E-07		1.38	[1.17-1.63]	"Ilumina [493,609]"	N
3/30/2009	19300499	Takeuchi	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose"	Warfarin maintenance dose	"1,053 individuals"	588 individuals	10q23.33	CYP2C9	rs1799853-?	rs1799853	0.11	1.00E-31		0.54	[0.45-0.63] mg/week decrease	"Illumina [325,997]"	N
3/30/2009	19300499	Takeuchi	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose"	Warfarin maintenance dose	"1,053 individuals"	588 individuals	16p11.2	VKORC1	rs9923231-T	rs9923231	0.4	0		0.97	[0.91-1.02] mg/week decrease	"Illumina [325,997]"	N
3/30/2009	19300499	Takeuchi	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose"	Warfarin maintenance dose	"1,053 individuals"	588 individuals	10q23.33	CYP2C9	rs1057910-?	rs1057910	0.07	3.00E-79		1.11	[1.00-1.22] mg/week decrease	"Illumina [325,997]"	N
3/30/2009	19300499	Takeuchi	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose"	Warfarin maintenance dose	"1,053 individuals"	588 individuals	19p13.12	CYP4F2	rs2108622-?	rs2108622	0.24	3.00E-10		0.21	[0.14-0.27] mg/week increase	"Illumina [325,997]"	N
3/31/2009	19300500	Wilk	20-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19300500?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study	Pulmonary function measures	"7,691 individuals"	835 individuals	4q31.22	HHIP	rs13147758-G	rs13147758	0.39	8.00E-11		0.1	[NR] % increase in FEV1/FVC ratio	"Affymetrix [2,540,223] (imputed)"	N
4/1/2009	19303062	Tanaka	18-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations"	Folate pathway vitamin levels	"2,934 individuals"	686 individuals	11q12.1	TCN1	rs526934-A	rs526934	0.67	0.000002	(vitamin B12)	27.62	[11.65-43.59] pg/mL increase	Affymetrix and Illumina [~2.5 million] (imputed)	N
4/1/2009	19303062	Tanaka	18-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations"	Folate pathway vitamin levels	"2,934 individuals"	686 individuals	19q13.33	FUT2	rs602662-A	rs602662	0.53	3.00E-20	(vitamin B12)	49.77	[37.09-62.45] pg/ml increase	Affymetrix and Illumina [~2.5 million] (imputed)	N
4/1/2009	19303062	Tanaka	18-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations"	Folate pathway vitamin levels	"2,934 individuals"	686 individuals	3p14.1	PRICKLE2	rs153734-T	rs153734	0.84	0.000007	(folate)	0.29	[0.13-0.45] ng/ml increase	Affymetrix and Illumina [~2.5 million] (imputed)	N
4/1/2009	19303062	Tanaka	18-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations"	Folate pathway vitamin levels	"2,934 individuals"	686 individuals	1p36.12	ALPL	rs4654748-C	rs4654748	0.5	8.00E-18	(vitamin B6)	1.45	[0.90-2.00] ng/ml decrease	Affymetrix and Illumina [~2.5 million] (imputed)	N
4/1/2009	19303062	Tanaka	18-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations"	Folate pathway vitamin levels	"2,934 individuals"	686 individuals	10p13	CUBN	rs11254363-A	rs11254363	0.7	0.000001	(vitamin B12)	21.49	[7.71-35.27] pg/mL decrease	Affymetrix and Illumina [~2.5 million] (imputed)	N
3/31/2009	19287384	Kilpivaara	15-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19287384?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms	Myeloproliferative neoplasms	"324 cases, 2,999 controls"	NR	9p24.1	JAK2	rs10974944-?	rs10974944	NR	4.00E-20		3.1	[2.40-4.00]	"Affymetrix [62,775]"	N
3/31/2009	19287509	Cui	14-Mar-09	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/19287509?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome Wide Association Study of Determinants of Anti-cyclic Citrullinated Peptide Antibody Titer in Adults with Rheumatoid Arthritis	Anti-cyclic Citrullianted Peptide Antibody	531 individuals with rheumatoid arthritis	849 individuals with rheumatoid arthritis	6p21.32	"HLA-DRA, HLA-DR3,BTNL2"	rs1980493-?	rs1980493	0.13	5.00E-07		NR	NR	"Affymetrix [97,248]"	N
3/29/2009	19282985	Liu	13-Mar-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19282985?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche	Menarche (age at onset)	477 women	"854 siblings, 762 women, 1,387 Chinese women"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [379,319]"	N
3/30/2009	19278955	Tregouet	10-Mar-09	Blood	http://www.ncbi.nlm.nih.gov/pubmed/19278955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common susceptibility allele are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach	Venous thromboembolism	"419 cases, 1,228 controls"	"1,757 cases, 1,480 controls"	9q34.2	ABO	rs505922-C	rs505922	0.35	4.00E-15		1.81	[1.56-2.11]	"Illumina [291,872]"	N
3/28/2009	19270707	Birnbaum	8-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19270707?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24	Nonsyndromic cleft lip with or without cleft palate	"224 cases, 383 controls"	"246 cases, 954 controls"	1q32.2	IRF6	rs642961-A	rs642961	NR	0.000002		NR	NR	"Illumina [521,176]"	N
3/28/2009	19270707	Birnbaum	8-Mar-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19270707?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24	Nonsyndromic cleft lip with or without cleft palate	"224 cases, 383 controls"	"246 cases, 954 controls"	8q24.21	"PVT1, GSDMC"	rs987525-A	rs987525	0.2	3.00E-24		2.57	[2.02-3.26]	"Illumina [521,176]"	N
3/24/2009	19268274	Liu	4-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19268274?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association and Replication Studies Identified TRHR as an Important Gene for Lean Body Mass	Body mass (lean)	"1,000 individuals"	"1,488 individuals, 1,972 family members, 2,955 Chinese individuals"	8q23.1	TRHR	rs7832552-T	rs7832552	0.32	4.00E-10		0.1	[0.04-0.16] kg increase	"Affymetrix [379,319]"	N
3/24/2009	19268276	Vink	4-Mar-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19268276?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Study of Smoking Initiation and Current Smoking	Smoking behavior	"3,540 individuals"	"6,405 individuals, 824 twin pairs"	NR	NR	NR		NR	NS	NS	NR	NR	"Perlegen [427,037]"	N
3/28/2009	19259986	Hattori	2-Mar-09	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/19259986?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Preliminary genome-wide association study of bipolar disorder in the Japanese population	Bipolar disorder	"107 cases, 107 controls"	"395 cases, 409 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [88,671]"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	3q13.12	BBX	rs6437740-?	rs6437740	0.24	2.00E-07	(CPD)	0.1	[NR] fewer cigarettes per day	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	16p13.2	Intergenic	rs3112740-?	rs3112740	0.86	0.000006	(CPDBI)	2.16	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	19p12	ZNF505	rs10411195-?	rs10411195	0.03	0.000006	(CPD)	0.21	[NR] fewer cigarettes per day	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	Xq23	TRPC5	rs7050529-?	rs7050529	0.07	0.000006	(CPD)	0.06	[NR] fewer cigarettes per day	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	17p13.2	CAMKK1	rs758642-?	rs758642	0.34	0.000007	(CPD)	0.08	[NR] more cigarettes per day	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	3q27.2	Intergenic	rs6444087-?	rs6444087	0.26	0.000009	(EVNV)	1.28	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	1p22.3	AK002179	rs7553864-?	rs7553864	0.39	0.000003	(SMKDU)	0.08	[NR] more years	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	13q33.1	Intergenic	rs912969-?	rs912969	0.07	0.000008	(SMKDU)	0.14	[NR] fewer years	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	4q28.1	Intergenic	rs950063-?	rs950063	0.39	0.000009	(SMKDU)	0.08	[NR] fewer years	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	5q14.3	LOC133789	rs933688-?	rs933688	0.17	0.000006	(EVNV)	1.48	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	14q24.1	ACTN1	rs2268983-?	rs2268983	0.51	0.000007	(CPDBI)	1.52	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	Xp11.3	MAOA	rs3027409-?	rs3027409	0.95	0.000007	(CPDBI)	1.73	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	7p15.2	Intergenic	rs886716-?	rs886716	0.69	0.000008	(CPDBI)	1.52	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	18q11.2	CABLES1	rs11082304-?	rs11082304	0.49	0.000006	(SMKAGE)	0.03	[NR] years older	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	4q31.1	SET7	rs17050782-?	rs17050782	0.21	0.000008	(SMKAGE)	0.03	[NR] years older	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	1p35.2	Intergenic	rs910696-?	rs910696	0.31	0.000003	(CPD)	0.08	[NR] more cigarettes per day	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	3q24	Intergenic	rs800082-?	rs800082	0.42	0.000003	(PKYRS)	0.12	[NR] more pack years	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	12q21.2	Intergenic	rs1402279-?	rs1402279	0.95	0.000005	(EVNV)	1.51	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	9p21.2	Intergenic	rs1889899-?	rs1889899	0.37	0.000006	(EVNV)	1.26	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	9q31.1	Intergenic	rs10989661-?	rs10989661	0.74	0.000006	(CIGSTAT)	1.68	[NR]	"Illumina [~518,000] (pooled)"	N
4/1/2009	19247474	Caporaso	27-Feb-09	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide and candidate gene association study of cigarette smoking behaviors	Smoking behavior	"4,611 individuals (2,617 smokers)"	NR	12q21.33	Intergenic	rs1847461-?	rs1847461	0.94	0.000008	(CIGSTAT)	1.8	[NR]	"Illumina [~518,000] (pooled)"	N
3/18/2009	19252134	Pezzolesi	27-Feb-09	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19252134?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes Mellitus	Diabetic nephropathy	"820 cases, 885 controls"	"1,304 individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [359,193]"	N
3/18/2009	19242412	Gu	25-Feb-09	Nature	http://www.ncbi.nlm.nih.gov/pubmed/19242412?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease	Cystic fibrosis severity	"160 severe lung disease patients, 160 mild lung disease patients (all homozygous for CFTR deltaF508 variant)"	"101 severe lung disease patients, 381 mild lung disease patients, 1,118 family members"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [100,198] (pooled)"	N
3/18/2009	19249006	Xiong	25-Feb-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19249006?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association and Follow-Up Replication Studies Identified ADAMTS18 and TGFBR3 as Bone Mass Candidate Genes in Different Ethnic Groups	Bone mineral density	"1,000 white individuals"	"4,925 white individuals, 350 Chinese hip fracture cases, 350 Chinese controls, 2,955 Chinese individuals, 908 West African men"	16q23.1	ADAMTS18	rs11864477-C	rs11864477	0.12	2.00E-08	(hip BMD)	1	% [NR] of variance explained	"Affymetrix [379,319]"	N
3/18/2009	19249006	Xiong	25-Feb-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19249006?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association and Follow-Up Replication Studies Identified ADAMTS18 and TGFBR3 as Bone Mass Candidate Genes in Different Ethnic Groups	Bone mineral density	"1,000 white individuals"	"4,925 white individuals, 350 Chinese hip fracture cases, 350 Chinese controls, 2,955 Chinese individuals, 908 West African men"	1p22.2	TGFBR3	rs17131547-A	rs17131547	0.01	0.000001	(spine BMD)	1.2	% [NR] of variance explained	"Affymetrix [379,319]"	N
3/1/2009	19230858	Schrauwen	18-Feb-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19230858?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis	Otosclerosis	"302 cases, 302 controls"	"847 cases, 872 controls"	7q22.1	RELN	rs3914132-?	rs3914132	0.23	2.00E-08		1.54	[1.32-1.79]	"Illumina [~555,000] (pooled)"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	3p22.2	SCN5A	rs7638909-G	rs7638909	0.4	0.000002	(PR interval)	4.8	[2.84-6.76] ms increase	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	2q31.1	Intergenic	rs2461751-G	rs2461751	0.44	0.000008	(PR interval)	4.54	[2.58-6.50] ms increase	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	3p22.2	SCN5A	rs2070488-A	rs2070488	0.33	0.000004	(PR interval)	5	[2.84-7.16] ms decrease	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	4p16.1	MSX1	rs2008242-?	rs2008242	0.15	0.000003	(PR segment)	NR	NR	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	1q32.1	NR	rs7512898-?	rs7512898	0.41	0.000005	(PR segment)	NR	NR	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	4q31.3	NR	rs17030434-?	rs17030434	0.43	0.000005	(P wave duration)	NR	NR	"Affymetrix [338,049]"	N
5/7/2009	19389651	Smith	15-Feb-09	Heart Rhythm	http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae	Electrocardiographic conduction measures	"1,262 Kosraen individuals"	NR	6p12.2	NR	rs283566-?	rs283566	0.16	0.000009	(P wave duration)	NR	NR	"Affymetrix [338,049]"	N
2/28/2009	19219042	Zheng	15-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19219042?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1	Breast cancer	"1,505 Chinese cases, 1,522 Chinese controls"	"1,554 Chinese cases, 1,576 Chinese controls"	6q25.1	C6orf97	rs2046210-A	rs2046210	0.37	2.00E-15		1.29	[1.21-1.37]	"Affymetrix [up to 607,728]"	N
2/28/2009	19221038	Soranzo	12-Feb-09	Blood	http://www.ncbi.nlm.nih.gov/pubmed/19221038?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"A novel variant on chromosome 7Q22.3 associated with mean platelet volume, counts and function"	Mean platelet volume	"1,221 individuals"	"7,365 individuals"	7q22.3	Intergenic	rs342293-G	rs342293	0.45	1.00E-24		0.02	[0.014-0.018] log fl increase	"Affymetrix [361,352]"	N
3/1/2009	19198612	Erdmann	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198612?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New susceptibility locus for coronary artery disease on chromosome 3q22.3	Coronary artery disease	"6,990 cases, 8,955 controls"	"12,417 cases, 12,411 controls"	12q24.31	"HNF1A,C12orf43"	rs2259816-T	rs2259816	0.36	5.00E-07		1.08	[1.05-1.11]	"Affymetrix [567,119]"	N
3/1/2009	19198612	Erdmann	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198612?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New susceptibility locus for coronary artery disease on chromosome 3q22.3	Coronary artery disease	"6,990 cases, 8,955 controls"	"12,417 cases, 12,411 controls"	3q22.3	MRAS	rs9818870-T	rs9818870	0.15	7.00E-13		1.15	[1.11-1.19]	"Affymetrix [567,119]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	2q12.1	IL1RL1	rs1420101-A	rs1420101	0.41	5.00E-14	(European)	6.4	[4.7-8.1] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	12q24.12	SH2B3	rs3184504-T	rs3184504	0.38	7.00E-19	(European)	7.6	[5.9-9.3] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	5q31.1	IL5	rs4143832-C	rs4143832	0.16	1.00E-10	(European)	7.1	[4.9-9.2] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	6p21.32	MHC	rs2269426-T	rs2269426	0.76	0.000003	(European)	4.6	[2.7-6.6] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	2q34	IKZF2	rs12619285-G	rs12619285	0.74	5.00E-10	(European)	6.3	[4.3-8.3] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	5q22.1	"WDR36, TSLP"	rs2416257-G	rs2416257	0.85	0.000001	(European)	6.1	[3.7-8.6] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198610	Gudbjartsson	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction	Plasma eosinophil count	"9,392 individuals"	"12,118 individuals"	3q21.3	GATA2	rs4857855-T	rs4857855	0.82	9.00E-17	(European)	9.4	[7.2-11.6] % standard unit increase	"Illumina [312,179]"	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	1p32.3	PCSK9	rs11206510-T	rs11206510	0.81	1.00E-08		1.15	[1.10-1.21]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	19p13.2	LDLR	rs1122608-G	rs1122608	0.75	2.00E-09		1.15	[1.10-1.20]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	21q22.11	"SLC5A3, MRPS6, KCNE2"	rs9982601-T	rs9982601	0.13	6.00E-11		1.2	[1.14-1.27]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	10q11.21	CXCL12	rs1746048-C	rs1746048	0.84	7.00E-09		1.17	[1.11-1.24]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	9p21.3	"CDKN2A, CDKN2B"	rs4977574-G	rs4977574	0.56	3.00E-44		1.29	[1.25-1.34]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	6p24.1	PHACTR1	rs12526453-C	rs12526453	0.65	1.00E-09		1.12	[1.08-1.17]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	2q33.1	WDR12	rs6725887-C	rs6725887	0.14	1.00E-08		1.17	[1.11-1.23]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	1p13.3	"CELSR2, PSRC1, SORT1"	rs646776-T	rs646776	0.81	8.00E-12		1.19	[1.13-1.26]	Affymetrix [~2.5 million] (imputed)	N
3/1/2009	19198609	Kathiresan	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants	Myocardial infarction (early onset)	"2,967 cases, 3,075 controls"	"9,746 cases, 9,746 controls"	1q41	MIA3	rs17465637-C	rs17465637	0.72	1.00E-09		1.14	[1.10-1.19]	Affymetrix [~2.5 million] (imputed)	N
4/1/2009	19198611	Tregouet	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198611?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease	Coronary artery disease	"1,926 cases, 2,938 controls"	"7,073 cases, 7,325 controls"	6q25.3	"SLC22A3,LPAL2,LPA"	4-SNP haplotype-1	"rs7767084,rs10755578,rs2048327,rs3127599"	0.16	1.00E-09	(CTTG)	1.2	[1.13-1.28]	"Affymetrix [~500,000]"	N
4/1/2009	19198611	Tregouet	8-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198611?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease	Coronary artery disease	"1,926 cases, 2,938 controls"	"7,073 cases, 7,325 controls"	6q25.3	"SLC22A3,LPAL2,LPA"	4-SNP haplotype-2	"rs2048327,rs3127599,rs7767084,rs10755578"	0.02	4.00E-15	(CCTC)	1.82	[1.57-2.12]	"Affymetrix [~500,000]"	N
2/28/2009	19198613	Gudmundsson	6-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198613?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations	Thyroid cancer	"192 cases, 37,196 controls"	"432 cases, 1,727 controls"	14q13.3	NKX2-1	rs944289-T	rs944289	0.57	2.00E-09		1.37	[1.24-1.52]	"Illumina [304,083]"	N
2/28/2009	19198613	Gudmundsson	6-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19198613?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations	Thyroid cancer	"192 cases, 37,196 controls"	"432 cases, 1,727 controls"	9q22.33	FOXE1	rs965513-A	rs965513	0.34	2.00E-27		1.75	[1.59-1.94]	"Illumina [304,083]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	12q24.31	SPPL3	rs1039302-T	rs1039302	0.36	0.000005	(CRP)	0.21	[NR] mg/L increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	12p13.33	"ENSG00000118975, FKBP4"	rs10848704-C	rs10848704	0.35	0.000002	(TSH)	0.29	[NR] mIU/L decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	5q35.3	MGAT1	rs655601-A	rs655601	0.47	0.000005	(HDL-C)	0.23	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	19q13.32	"MGC2650, BLOC1S3, XTP7"	rs2159324-T	rs2159324	0.44	4.00E-07	(LDL-C)	0.21	[NR] mg/dL decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	5q13.3	"COL4A3BP, HMGCR"	rs3846663-T	rs3846663	0.39	0.000001	(LDL-C)	0.21	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	10p15.3	ADARB2	rs6560749-T	rs6560749	0.14	0.000002	(BMI)	0.32	[NR] kg/m2 decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	7p14.1	Intergenic	rs10486715-A	rs10486715	0.07	0.000003	(height)	0.44	[NR] inch decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	3q25.33	SCHIP1	rs2222328-C	rs2222328	0.32	8.00E-07	(WC)	0.22	[NR] inch decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	9p21.3	Intergenic	rs613391-G	rs613391	0.49	0.000005	(WC)	0.2	[NR] inch increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	9p21.3	Intergenic	rs2225614-C	rs2225614	0.5	0.000003	(weight)	0.21	[NR] lb. decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	2q22.2	ARHGAP15	rs10928195-C	rs10928195	0.08	0.000004	(weight)	0.36	[NR] lb. decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	7q34	TRIM24	rs1874326-G	rs1874326	0.47	0.000009	(weight)	0.22	[NR] lb. increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	20q13.12	Intergenic	rs6066084-A	rs6066084	0.06	0.000002	(% body fat)	0.85	[NR] % increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	10p15.3	ADARB2	rs6560749-T	rs6560749	0.14	0.000008	(% body fat)	0.34	[NR] % decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	6p22.3	Intergenic	rs10498712-G	rs10498712	0.25	0.000009	(HDL-C)	0.23	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	19q13.32	"MGC2650, BLOC1S3, XTP7"	rs2159324-T	rs2159324	0.44	0.000002	(CRP)	0.19	[NR] mg/L decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	19q13.32	"TOMMM40, APOC2, APOE, APOC4, APOC1"	rs4420638-G	rs4420638	0.21	3.00E-07	(TC)	0.28	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	5q13.3	"COL4A3BP, HMGCR"	rs3846663-T	rs3846663	0.39	0.000006	(TC)	0.19	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	10p13	ITGA8	rs7895372-G	rs7895372	0.04	0.000006	(TC)	0.35	[NR] mg/dL decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	7p21.3	Intergenic	rs17157663-A	rs17157663	0.32	0.000009	(TC)	0.18	[NR] mg/dL decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	11q23.3	Intergenic	rs7396835-T	rs7396835	0.32	1.00E-09	(TG)	0.23	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	4q21.21	Intergenic	rs10518224-A	rs10518224	0.23	0.000007	(TG)	0.19	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	19q13.32	"TOMM40, APOC2, APOE, APOC4, APOC1"	rs4420638-G	rs4420638	0.21	0.000005	(TG)	0.22	[NR] mg/dL increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	10p12.33	CACNB2	rs7069923-C	rs7069923	0.49	0.000001	(SBP)	0.19	[NR] mm Hg increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	7q36.3	UBE3C	rs2527866-C	rs2527866	0.23	0.000003	(SBP)	0.27	[NR] mm Hg decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	5q35.1	Intergenic	rs254893-A	rs254893	0.06	0.000006	(DBP)	0.58	[NR] mm Hg decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	10p13	CUBN	rs10508517-A	rs10508517	0.43	0.000006	(DBP)	0.18	[NR] mm Hg decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	9q22.33	"HEMGN, C9ORF156"	rs755109-C	rs755109	0.23	0.000001	(TSH)	0.31	[NR] mIU/L decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	7p22.2	SDK1	rs6462411-C	rs6462411	0.2	0.000001	(TSH)	0.36	[NR] mIU/L decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	19q13.32	"TOMM40, APOC2, APOE, APOC4, APOC1"	rs4420638-G	rs4420638	0.21	0.000002	(CRP)	0.28	[NR] mg/L decrease	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	2p23.3	"ENSG0000173957, UBXD4, FKBP1B, FLJ21945"	rs7561273-A	rs7561273	0.35	0.000006	(CRP)	0.22	[NR] mg/L decrease]	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	12q24.13	Intergenic	rs11066587-G	rs11066587	0.16	0.000005	(CRP)	0.26	[NR] mg/L increase	"Affymetrix [408,775]"	N
10/15/2009	19197348	Lowe	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae	Quantitative traits	"Up to 2,906 Micronesian individuals"	NR	6q16.2	Intergenic	rs6909430-G	rs6909430	0.08	0.000008	(TSH)	0.49	[NR] mIU/L decrease	"Affymetrix [408,775]"	N
8/21/2009	19197363	Need	6-Feb-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19197363?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide investigation of SNPs and CNVs in schizophrenia	Schizophrenia	"871 European ancestry cases, 863 European ancestry controls"	"1,460 European ancestry cases, 12,995 European ancestry controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [312,565] (pooled)"	N
2/27/2009	19196962	Garcia-Barcelo	5-Feb-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19196962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease	Hirschsprung's disease	"181 Chinese cases, 346 Chinese controls"	"190 Chinese cases, 510 Chinese controls"	8p12	NRG1	rs16879552-G	rs16879552	0.39	2.00E-08		1.68	[1.40-2.00]	"Affymetrix [293,836]"	N
2/27/2009	19196962	Garcia-Barcelo	5-Feb-09	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19196962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease	Hirschsprung's disease	"181 Chinese cases, 346 Chinese controls"	"190 Chinese cases, 510 Chinese controls"	10q21.1	"RET, GALNACT-2, RASGEF1A"	rs2742234-T	rs2742234	NR	4.00E-18		NR	NR	"Affymetrix [293,836]"	N
3/31/2009	19193627	Chio	4-Feb-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19193627?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"553 cases, 2,338 controls"	"3,149 cases, 3,335 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [545,066]"	N
2/27/2009	19188921	Liu	3-Feb-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19188921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15	Smoking behavior	"417 Caucasian males, 423 Caucasian females"	"412 African American males, 839 African American females, 3,491 Caucasian males, 4,132 Caucasian females"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [379,319]"	N
2/28/2009	19187332	Kim	1-Feb-09	Clin Exp Allergy	http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis	Asthma (toluene diisocyanate-induced)	"84 Korean cases, 263 Korean controls"	NR	10q21.3	CTNNA3	rs10762058-G	rs10762058	0.25	0.000006		5	[2.36-10.6]	"Affymetrix [312,978]"	N
2/28/2009	19187332	Kim	1-Feb-09	Clin Exp Allergy	http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis	Asthma (toluene diisocyanate-induced)	"84 Korean cases, 263 Korean controls"	NR	13q12.13	Intergenic	rs9319321-T	rs9319321	0.29	0.000003		5.2	[2.47-10.92]	"Affymetrix [312,978]"	N
2/28/2009	19187332	Kim	1-Feb-09	Clin Exp Allergy	http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis	Asthma (toluene diisocyanate-induced)	"84 Korean cases, 263 Korean controls"	NR	9p21.3	Intergenic	rs16937883-G	rs16937883	0.02	0.000007		5.29	[2.41-11.61]	"Affymetrix [312,978]"	N
2/27/2009	19207018	Kim	1-Feb-09	Pharmacogenomics	http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of acute post-surgical pain in humans	Pain	"60 females, 52 males"	NR	19p12	"LOC400680, ZNF429"	rs2562456-?	rs2562456	NR	2.00E-10	(onset time of analgesia)	NR	NR	"Affymetrix [374,975]"	N
2/27/2009	19207018	Kim	1-Feb-09	Pharmacogenomics	http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of acute post-surgical pain in humans	Pain	"60 females, 52 males"	NR	11q23.3	NR	rs17122021-?	rs17122021	NR	7.00E-07	(maximum post-operative pain rating)	NR	NR	"Affymetrix [374,975]"	N
2/27/2009	19207018	Kim	1-Feb-09	Pharmacogenomics	http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of acute post-surgical pain in humans	Pain	"60 females, 52 males"	NR	1p21.3	NR	rs6693882-?	rs6693882	NR	0.000002	(post-operative pain onset time)	NR	NR	"Affymetrix [374,975]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	14q32.13	"LOC122509, FAM14B"	rs7157940-?	rs7157940	0.46	0.000003	(weight)	0.12	[0.07-0.17] kg increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	2q31.1	Intergenic	rs7590983-?	rs7590983	0.05	0.000006	(BMI)	0.46	[0.26-0.66] kg/m2 increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	7q22.1	ZNF498	rs7792939-?		0.15	0.000006	(hip circumference)	0.26	[0.15-0.37] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	5q33.3	SGCD	rs157350-?		0.11	0.000006	(hip circumference)	0.31	[0.18-0.44] mm decrease	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	5q33.2	"AMPA1, GRIA1"	rs12658202-?	rs12658202	0.45	0.000009	(height)	0.11	[0.06-0.16] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	2p22.3	CRIM1	rs1863080-?	rs1863080	0.1	0.000008	(brachial circumference)	0.31	[0.17-0.45] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	7q22.1	ZNF498	rs7792939-?		0.15	0.000004	(weight)	0.26	[0.15-0.37] kg increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	7q22.1	ZNF498	rs7792939-?	"rs7792939,rs7792939,rs7792939"	0.15	0.000005	(brachial circumference)	0.26	[0.15-0.37] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	5q33.3	SGCD	rs157350-?	rs157350	0.11	0.000004	(brachial circumference)	0.31	[0.18-0.44] mm decrease	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	13q14.3	XTP498	rs7792939-?	rs7792939	0.28	0.000006	(brachial circumference)	0.17	[0.10-0.24] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	16p11.2	SEZ6L2	rs4787483-?	rs4787483	0.34	0.000002	(waist cirumference)	0.16	[0.09-0.23] mm increase	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	14q23.3	MAX	rs7158173-?	rs7158173	0.48	0.000004	(waist circumference)	0.11	[0.06-0.16] mm decrease	"Illumina [316,730]"	N
3/30/2009	19260139	Polasek	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of anthropometric traits in Korcula Island, Croatia"	Anthropometric traits	898 individuals	NR	1p36.32	Intergenic	rs7513590-?	rs7513590	0.1	0.000005	(height)	0.31	[0.17-0.45] mm decrease	"Illumina [316,730]"	N
2/25/2009	19182806	Stefansson	1-Feb-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19182806?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variant in the sequence of the LINGO1 gene confers risk of essential tremor	Essential tremor	"452 cases, 14,378 controls"	"300 cases, 1,419 controls"	15q24.3	LINGO1	rs9652490-G	rs9652490	0.23	1.00E-09		1.55	[1.35-1.79]	"Illumina [305,624]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	6q16.3	GRIK2	rs12207601-G	rs12207601	0.16	0.000002	(fibrinogen)	0.26	[0.15-0.37] g/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	21q22.3	PKNOX1	rs2839619-G	"rs2839619,rs2839619"	0.4	0.000008	(total cholesterol)	0.13	[0.07-0.19] mmol/L increase	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	12q24.23	KSR2	rs10444502-C	rs10444502	0.28	0.000006	(total cholesterol)	0.17	[0.10-0.24] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	Xp22.31	Neuroligin 4	rs7885458-G	rs7885458	0.24	0.000003	(fibrinogen)	0.23	[0.13-0.33] g/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	4p16.1	SLC2A9	rs13129697-C	rs13129697	0.25	1.00E-09	(uric acid)	0.29	[0.21-0.37] umol/l decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	18q12.3	SLC14A2	rs10502868-G	rs10502868	0.08	0.000007	(albumin)	0.04	[0.21-0.51] g/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	4q13.1	LPHN3	rs4599440-A	rs4599440	0.23	0.000002	(HDL cholesterol)	0.2	[0.12-0.28] mmol/L increase	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	12q12	Intergenic	rs871392-A	rs871392	0.15	0.000003	(HDL cholesterol)	0.26	[0.15-0.37] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	16q13	CETP	rs7499892-A	rs7499892	0.16	0.000009	(HDL cholesterol)	0.24	[0.14-0.34] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	12q24.23	KSR2	rs4767631-A	rs4767631	0.31	6.00E-07	(LDL cholesterol)	0.12	[0.11-0.23] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	21q22.3	PKNOX1	rs2839619-G		0.4	0.000008	(LDL cholesterol)	0.13	[0.08-0.18] mmol/L increase	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	4q23	RAP1GDS1	rs10516430-A	rs10516430	0.28	0.000006	(triglycerides)	0.16	[0.09-0.23] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	4q12	USP46	rs346923-A	rs346923	0.13	0.000002	(triglycerides)	0.28	[0.17-0.39] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	4q31.23	NR3C2	rs1490453-A	rs1490453	0.17	0.000003	(fibrinogen)	0.25	[0.15-0.35] g/L increase	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	20p12.1	PCSK2	rs6044777-A	rs6044777	0.17	0.000008	(fibrinogen)	0.23	[0.13-0.33] g/L increase	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	12q21.33	Intergenic	rs10777332-A	rs10777332	0.11	0.000005	(total cholesterol)	0.24	[0.14-0.34] mmol/L decrease	"Illumina [316,730]"	N
3/31/2009	19260141	Zemunik	1-Feb-09	Croat Med J	http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genome-wide association study of biochemical traits in Korcula Island, Croatia"	Biochemical measures	898 individuals	NR	Xq23	ZCCHC16	rs5982533-G	rs5982533	0.22	0.000007	(triglycerides)	0.23	[0.13-0.33] mmol/L decrease	"Illumina [316,730]"	N
2/25/2009	19181680	Timpson	30-Jan-09	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19181680?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in the region around Osterix are associated with bone mineral density and growth in childhood	Bone mineral density	"1,418 children, 135 adults"	"3,875 children"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [up to 315,807]"	N
2/28/2009	19185284	Ferrucci	29-Jan-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19185284?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study"	Plasma carotenoid and tocopherol levels	"1,191 individuals"	"2,751 individuals"	16q23.2	BCMO1	rs6564851-G	rs6564851	0.39	2.00E-24	(beta-carotene)	0.15	[0.120-0.177] umol/L increase	"Illumina [~500,451] (pooled)"	N
2/28/2009	19185284	Ferrucci	29-Jan-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19185284?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study"	Plasma carotenoid and tocopherol levels	"1,191 individuals"	"2,751 individuals"	11q23.3	APOA5	rs12272004-A	rs12272004	0.07	8.00E-10	(alpha-tocopherol)	0.07	[0.049-0.095] umol/L increase	"Illumina [~500,451] (pooled)"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	10p14	Intergenic	rs10508343-A	rs10508343	0.04	0.000008		3.81	[1.40-10.40]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	10q26.12	intergenic	rs2901286-A	rs2901286	0.03	0.000004		4.66	[1.58-13.7]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	7p21.2	DGKB	rs6971925-T	rs6971925	0.02	0.000003		13.91	[2.72-70.92]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	11p15.1	intergenic	rs7128311-C	rs7128311	0.03	0.000005		13.9	[2.72-71.1]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	11q21	MAML2	rs7115578-A	rs7115578	0.64	0.000008		1.86	[1.23-2.79]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	10p12.33	ST8SIA6	rs359312-T	rs359312	0.04	9.00E-08		3.91	[1.52-10.10]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	4q31.21	IL15	rs17007695-C	rs17007695	0.1	9.00E-07		2.67	[1.53-4.68]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	7p14.2	ELMO1	rs4723619-C	rs4723619	0.07	0.000003		3.01	[1.50-6.03]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	6q25.3	intergenic	rs35229355-T	rs35229355	0.03	0.000005		7.24	[2.46-21.30]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	5p13.2	LMBRD2	rs267759-A	rs267759	0.05	0.000007		3.23	[1.52-6.87]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	2q33.1	C2orf47	rs1569175-T	rs1569175	0.11	9.00E-07		2.73	[1.52-4.93]	"Affymetrix [476,796]"	N
2/26/2009	19176441	Yang	28-Jan-09	JAMA	http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia	Treatment response for acute lymphoblastic leukemia	487 children	NR	20q13.12	NCOA3	rs6125048-T	rs6125048	0.04	0.000002		2.73	[1.08-6.88]	"Affymetrix [476,796]"	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	1p31.3	IL23R	rs2201841-G	rs2201841	0.3	3.00E-08		1.13	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	12q13.2	"IL23A, STAT2"	rs2066808-A	rs2066808	0.93	1.00E-09		1.34	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	6q23.3	TNFAIP3	rs610604-G	rs610604	0.32	9.00E-12		1.19	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	5q33.1	TNIP1	rs17728338-A	rs17728338	0.054	1.00E-20		1.59	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	6p21.33	HLA-C	rs12191877-T	rs12191877	0.15	1.00E-100		2.64	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	5q31.1	IL13	rs20541-G	rs20541	0.79	5.00E-15		1.27	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	5q33.3	IL12B	rs2082412-G	rs2082412	0.8	2.00E-28		1.44	[NR]	Perlegen [~2.5 million] (imputed)	N
2/6/2009	19169254	Nair	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways	Psoriasis	"1,359 cases, 1,400 controls"	"5,048 cases, 5,041 controls"	9q34.13	TSC1	rs1076160-T	rs1076160	0.48	0.000006		1.09	[NR]	Perlegen [~2.5 million] (imputed)	N
2/7/2009	19169255	Zhang	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21	Psoriasis	"1,139 Chinese cases, 1,132 Chinese controls"	"5,721 Chinese cases, 7,340 Chinese controls"	1q21.3	"LCE3D, LCE3A"	rs4085613-A	rs4085613	0.43	7.00E-30		1.32	[1.25-1.39]	"Illumina [494,902]"	N
2/7/2009	19169255	Zhang	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21	Psoriasis	"1,139 Chinese cases, 1,132 Chinese controls"	"5,721 Chinese cases, 7,340 Chinese controls"	5q33.3	IL12B	rs3213094-A	rs3213094	0.45	3.00E-26		1.28	[1.23-1.35]	"Illumina [494,902]"	N
2/7/2009	19169255	Zhang	25-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21	Psoriasis	"1,139 Chinese cases, 1,132 Chinese controls"	"5,721 Chinese cases, 7,340 Chinese controls"	6p21.33	MHC	rs1265181-?	rs1265181	NR	NS	NS	22.62		"Illumina [494,902]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	19q13.33	Intergenic	rs3810265-?	rs3810265	0.07	0.000004		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	20p13	SMOX	rs16989303-?	rs16989303	0.21	0.000006		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	1q32.1	PKP1	rs860554-?	rs860554	0.05	5.00E-08		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	6q25.1	PLEKHG1	rs9372078-?	rs9372078	0.11	5.00E-07		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	8p21.1	CLU	rs17466684-?	rs17466684	0.09	7.00E-07		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	12p13.31	TMEM16B	rs12579350-?	rs12579350	0.01	4.00E-09		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	12q24.33	Intergenic	rs7299940-?	rs7299940	0.29	0.000007		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	3p26.1	GRM7	rs3749380-?	rs3749380	0.25	0.000002		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	14q23.1	Intergenic	rs4901869-?	rs4901869	0.02	0.000006		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	21q21.1	USP25	rs2823455-?	rs2823455	0.03	0.000009		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	1p13.3	Intergenic	rs12061304-?	rs12061304	0.1	0.000001		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	12q13.13	CALCOCO1	rs941184-?	rs941184	0.03	3.00E-07		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	13q32.1	Intergenic	rs9302001-?	rs9302001	0.2	3.00E-07		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	17q25.1	SDK2	rs3816995-?	rs3816995	0.03	2.00E-07		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	5q21.1	Intergenic	rs4702982-?	rs4702982	0.16	0.000006		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	6p12.3	TNFRSF21	rs2103868-?	rs2103868	0.26	0.000005		NR	NR	"Affymetrix [253,903]"	N
2/26/2009	19165232	Otowa	23-Jan-09	J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of panic disorder in the Japanese population	Panic disorder	"200 Japanese cases, 200 Japanese controls"	NR	12q12	Intergenic	rs2731006-?	rs2731006	0.29	0.000004		NR	NR	"Affymetrix [253,903]"	N
2/25/2009	19165155	Ling	22-Jan-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19165155?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Linkage and Association Anaylses to Identify Genes Influencing Adiponectin Levels: The GEMS Study	Adiponectin levels	"997 cases, 989 controls"	NR	5q35.2	Intergenic	rs7722022-?	rs7722022	NR	0.000009		NR	NR	"Affymetrix [398,625]"	N
2/25/2009	19165155	Ling	22-Jan-09	Obesity	http://www.ncbi.nlm.nih.gov/pubmed/19165155?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Linkage and Association Anaylses to Identify Genes Influencing Adiponectin Levels: The GEMS Study	Adiponectin levels	"997 cases, 989 controls"	NR	3q27.3	ADIPOQ	rs6773957-A	rs6773957	0.37	5.00E-08		NR	NR	"Affymetrix [398,625]"	N
3/3/2009	19151714	Meyre	18-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations	Obesity	"695 obese adults, 685 obese children, 731 lean adults, 685 lean children"	"1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children"	18q21.32	MC4R	rs17782313-C	rs17782313	0.18	5.00E-15	(children)	1.22	[1.05-1.40]	"Illumina [308,846]"	N
3/3/2009	19151714	Meyre	18-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations	Obesity	"695 obese adults, 685 obese children, 731 lean adults, 685 lean children"	"1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children"	18q11.2	NPC1	rs1805081-A	rs1805081	0.56	3.00E-07	(children)	1.33	[1.08-1.75]	"Illumina [308,846]"	N
3/3/2009	19151714	Meyre	18-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations	Obesity	"695 obese adults, 685 obese children, 731 lean adults, 685 lean children"	"1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children"	16q23.2	MAF	rs1424233-A	rs1424233	0.43	4.00E-13	(children)	1.12	[1.00-1.24]	"Illumina [308,846]"	N
3/3/2009	19151714	Meyre	18-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations	Obesity	"695 obese adults, 685 obese children, 731 lean adults, 685 lean children"	"1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children"	10p13	PTER	rs10508503-C	rs10508503	0.91	2.00E-07	(children)	1.56	[1.10-2.78]	"Illumina [308,846]"	N
3/3/2009	19151714	Meyre	18-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations	Obesity	"695 obese adults, 685 obese children, 731 lean adults, 685 lean children"	"1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children"	16q12.2	FTO	rs1421085-C	rs1421085	0.4	1.00E-28	(children)	1.39	[1.27-1.51]	"Illumina [308,846]"	N
1/21/2009	19148276	Tanaka	16-Jan-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19148276?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study	Plasma levels of polyunsaturated fatty acids	"1,210 individuals"	"1,076 individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [495,343]"	N
2/27/2009	19136949	Carrasquillo	11-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19136949?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease	Alzheimer's disease	"844 cases, 1,255 controls"	"1,547 cases, 1,209 controls"	Xq21.31	PCDH11X	rs2573905-?	rs2573905	0.46	2.00E-07		1.29	[1.17-1.42]	"Illumina [313,504]"	N
1/21/2009	19132087	Burgner	9-Jan-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19132087?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies novel and functionally related susceptibility loci for Kawasaki disease	Kawasaki disease	"107 cases, 134 controls"	"583 cases, 1,357 family members"	3q26.31	NAALADL2	rs17531088-T	rs17531088	0.44	0.000001		1.43	[1.32-1.53]	"Affymetrix [223,922]"	N
1/21/2009	19132087	Burgner	9-Jan-09	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19132087?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies novel and functionally related susceptibility loci for Kawasaki disease	Kawasaki disease	"107 cases, 134 controls"	"583 cases, 1,357 family members"	16q22.3	ZFHX3	rs7199343-T	rs7199343	0.3	0.000002		1.56	[1.33-1.92]	"Affymetrix [223,922]"	N
2/25/2009	19125160	Feulner	7-Jan-09	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19125160?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Examination of the current top candidate genes for AD in a genome-wide association study	Alzheimer's disease	"491 cases, 479 controls"	NR	19q13.32	"TOMM40, APOE"	rs157580-?	rs157580	NR	1.00E-40		NR	NR	"Illumina [~550,000]"	N
1/21/2009	19124843	Ober	7-Jan-09	J Lipid Res	http://www.ncbi.nlm.nih.gov/pubmed/19124843?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of plasma Lp(a)levels Identifies multiple genes on chromosome 6q	Plasma Lp (a) levels	357 individuals	"1,054 individuals"	6q25.3	LPA	rs6919346-?	rs6919346	0.16	4.00E-11		0.66	[mg/dl decrease]	"Affymetrix [290,327]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	12q15	"IFNG, IL26, IL22"	rs1558744-A	rs1558744	0.38	3.00E-12		1.35		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	7q31.1	"SLC26A3, DLD, LAMB1"	rs2158836-A	rs2158836	0.35	0.000007		1.21		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	7q31.1	Intergenic	rs4730273-?	rs4730273	0.7	0.000005		1.22		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	6p21.32	"BTNL2, HLA-DRA, HLA-DRB5, HLA-DRB1, HLA-DQA1, HLA-DQB1"	rs2395185-?	rs2395185	0.67	1.00E-16		1.52		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	12q15	IL26	rs2870946-G	rs2870946	0.055	5.00E-07		1.54		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	7q31.1	"SLC26A3, DLD, LAMB1"	rs4730276-?	rs4730276	0.39	0.000009		1.22		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	1p36.13	RNF186	rs3806308-?	rs3806308	0.63	7.00E-09		1.28		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	1p36.13	"OTUD3, PLA2G2E"	rs6426833-G	rs6426833	0.54	5.00E-13		1.37		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	1p31.3	IL23R	rs10889677-A	rs10889677	0.3	1.00E-08		1.29		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	7q31.1	"SLC26A3, DLD, LAMB1"	rs4598195-?	rs4598195	0.54	0.000001		1.23		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	9q21.32	Intergenic	rs668853-G	rs668853	0.39	0.000002		1.2		"Illumina [280,748]"	N
1/21/2009	19122664	Silverberg	4-Jan-09	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study	Ulcerative colitis	"1,022 cases, 2,503 controls"	"1,387 cases, 1,115 controls"	1p31.3	IL23R	rs11209026-?	rs11209026	0.93	1.00E-08		1.79		"Illumina [280,748]"	N
1/21/2009	19118814	Beecham	3-Jan-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease	Alzheimer's disease	"492 cases, 496 controls"	"238 cases, 220 controls"	1q42.2	DISC1	rs12044355-?	rs12044355	NR	0.000009		NR	NR	Illumina [~2.5 million] (imputed)	N
1/21/2009	19118814	Beecham	3-Jan-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease	Alzheimer's disease	"492 cases, 496 controls"	"238 cases, 220 controls"	12q13.11	FAM113B	rs11610206-?	rs11610206	NR	3.00E-07		NR	NR	Illumina [~2.5 million] (imputed)	N
1/21/2009	19118814	Beecham	3-Jan-09	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease	Alzheimer's disease	"492 cases, 496 controls"	"238 cases, 220 controls"	19q13.31	ZNF224	rs2061333-?	rs2061333	NR	0.000002		NR	NR	Illumina [~2.5 million] (imputed)	N
2/27/2009	19116933	Hinks	1-Jan-09	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/19116933?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis	Arthritis (juvenile idiopathic)	"279 cases, 184 controls"	"up to 654 cases, 1,847 controls"	1p13.1	VTCN1	rs12046117-?	rs12046117	0.09	0.000001		1.58	[1.29-1.94]	"Affymetrix [88,862]"	N
1/16/2009	19115949	Limou	1-Jan-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02).	AIDS progression	"275 HIV positive patients, 1,438 controls"	626 patients	6p21.33	"HCP5, MICB, MCCD1, BAT1, LTB, TNF"	rs2395029-G	rs2395029	0.03	3.00E-19		3.47	[2.39-5.04]	"Illumina [291,119]"	N
1/16/2009	19115949	Limou	1-Jan-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02).	AIDS progression	"275 HIV positive patients, 1,438 controls"	626 patients	6p21.33	HLA-C	rs10484554-T	rs10484554	0.13	6.00E-08		NR	NR	"Illumina [291,119]"	N
1/16/2009	19115949	Limou	1-Jan-09	J Infect Dis	http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02).	AIDS progression	"275 HIV positive patients, 1,438 controls"	626 patients	6p21.33	"ZNRD1, RNF39"	rs8321-G	rs8321	NR	5.00E-07		NR	NR	"Illumina [291,119]"	N
2/26/2009	19117981	Sun	1-Jan-09	Cancer Res	http://www.ncbi.nlm.nih.gov/pubmed/19117981?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variants at 22q13 are associated with prostate cancer risk	Prostate cancer	"1,235 aggressive cases, 1,599 controls"	"3,629 aggressive cases, 4,255 non-aggressive cases, 5,738 controls"	22q13.1	TNRC6B	rs9623117-C	rs9623117	0.21	5.00E-07		1.18	[1.11-1.26]	Affymetrix and Illumina [~2 million] (imputed)	N
1/14/2009	19114987	Zhang	31-Dec-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19114987?ordinalpos=17&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Singleton deletions throughout the genome increase risk of bipolar disorder	Bipolar disorder	"1,001 cases, 1,033 controls"	NR	Pending	Pending	Pending		Pending	Pending	Pending	Pending	Pending	"Affymetrix [51,757 CNVs]"	Y
1/14/2009	19114657	Wang	29-Dec-08	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/19114657?ordinalpos=13&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Whole-genome association study identifies STK39 as a hypertension susceptibility gene	Blood pressure	542 individuals	"6,583 individuals"	2q24.3	STK39	rs6749447-G	rs6749447	0.28	2.00E-07		1.9	[1.2-2.6] mm Hg increase in DBP	"Affymetrix [79,447]"	N
1/14/2009	19110211	Meisinger	24-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies three loci associated with mean platelet volume	Mean platelet volume	"1,606 individuals"	"8,617 individuals"	3p14.3	ARHGEF3	rs12485738-A	rs12485738	0.3	4.00E-27		0.02	[0.01-0.02] per log fl increase	"Affymetrix [335,152]"	N
1/14/2009	19110211	Meisinger	24-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies three loci associated with mean platelet volume	Mean platelet volume	"1,606 individuals"	"8,617 individuals"	12q24.31	WDR66	rs7961894-A	rs7961894	0.11	7.00E-48		0.03	[0.03-0.04] per log fl increase	"Affymetrix [335,152]"	N
1/14/2009	19110211	Meisinger	24-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies three loci associated with mean platelet volume	Mean platelet volume	"1,606 individuals"	"8,617 individuals"	17q11.2	TAOK1	rs2138852-C	rs2138852	0.47	7.00E-28		0.02	[0.01-0.02] per log fl decrease	"Affymetrix [335,152]"	N
2/4/2009	19107115	Muglia	23-Dec-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19107115?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts	Major depressive disorder	"1,359 cases, 1,782 controls"	NR	12p13.32	CCND2	rs4238010-G	rs4238010	0.02	0.000006		1.72		"Illumina and Affymetrix [494,678] (imputed)"	N
6/22/2009	19096518	Pare	19-Dec-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study"	Glycated hemoglobin levels	"14,618 Caucasian women"	455 Caucasian men and women	10q21.3	HK1	rs7072268-A	rs7072268	0.5	2.00E-25		0.05	[NR] % increase	"Illumina [337,343]"	N
6/22/2009	19096518	Pare	19-Dec-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study"	Glycated hemoglobin levels	"14,618 Caucasian women"	455 Caucasian men and women	8q24.11	SLC30A8	rs13266634-A	rs13266634	0.3	5.00E-08		0.02	[NR] % decrease	"Illumina [337,343]"	N
6/22/2009	19096518	Pare	19-Dec-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study"	Glycated hemoglobin levels	"14,618 Caucasian women"	455 Caucasian men and women	7p13	GCK	rs730497-A	rs730497	0.17	6.00E-12		0.03	[NR] % increase	"Illumina [337,343]"	N
6/22/2009	19096518	Pare	19-Dec-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study"	Glycated hemoglobin levels	"14,618 Caucasian women"	455 Caucasian men and women	2q24.3	G6PC2	rs1402837-A	rs1402837	0.23	5.00E-10		0.02	[NR] % increase	"Illumina [337,343]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.2	LRRC16A	rs2274089-?	rs2274089	NR	0.000005	(serum iron)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	HFE	rs1800562-?	rs1800562	NR	4.00E-11	(serum iron)	0.66	[0.46-0.86] SD increase	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	HFE	rs1800562-?	rs1800562	NR	1.00E-10	(serum transferrin)	0.68	[0.48-0.88] SD decrease	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	3q22.1	TF	rs3811647-?	rs3811647	NR	3.00E-15	(serum transferrin)	0.46	[0.34-0.58] SD decrease	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.2	LRRC16	rs2274089-?	rs2274089	NR	3.00E-07	(serum transferrin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	3q22.1	TOPBP1	rs2718812-?	rs2718812	NR	0.000001	(serum transferrin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	Xq24	KLHL13	rs2430212-?	rs2430212	NR	0.000002	(serum transferrin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.2	SLC17A1	rs17270561-?	rs17270561	NR	5.00E-07	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.2	SCGN	rs932316-?	rs932316	NR	0.000009	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	411 family members	NR	3q22.1	TF	rs1830084-A	rs1830084	0.36	1.00E-09	(serum transferrin)	0.43	[NR] SD increase	"Affymetrix [100,846]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	411 family members	NR	14q23.2	Q6ZUR9	rs973968-?	rs973968	NR	0.000003	(transferrin saturation)	NR	NR	"Affymetrix [100,846]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	411 family members	NR	6q22.33	RSPO3	rs972275-?	rs972275	NR	0.000002	(serum ferritin)	NR	NR	"Affymetrix [100,846]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	22q12.3	TMPRSS6	rs4820268-?	rs4820268	NR	0.000006	(serum iron)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	3q22.1	TF	rs1867504-?	rs1867504	NR	0.000002	(serum transferrin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	11p14.3	LUZP2	rs10500991-?	rs10500991	NR	0.000002	(serum transferrin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	HFE	rs1800562-?	rs1800562	NR	4.00E-15	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	HIST1H2BJ	rs13194491-?	rs13194491	NR	1.00E-08	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	BTN1A1	rs13194984-?	rs13194984	NR	6.00E-08	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.2	LRRC16	rs2274089-?	rs2274089	NR	8.00E-07	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	2p14	Q6ZNG6	rs1457451-?	rs1457451	NR	0.000003	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6p22.1	TRIM38	rs12216125-?	rs12216125	NR	0.000004	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	5p12	GHR	rs13188386-?	rs13188386	NR	0.000008	(transferrin saturation)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	6q25.3	WTAP	rs4516970-?	rs4516970	NR	0.000001	(serum ferritin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	7p14.1	Q4KMW4	rs29880-?	rs29880	NR	0.000007	(serum ferritin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	5q14.1	ARSB	rs2052550-?	rs2052550	NR	0.000008	(serum ferritin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	18q22.2	Intergenic	rs2660917-?	rs2660917	NR	0.000008	(serum ferritin)	NR	NR	"Illumina [315,887]"	N
1/14/2009	19084217	Benyamin	17-Dec-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels	Serum markers of iron status	459 twin pairs	NR	3q22.1	TF	rs1799852-?	rs1799852	0.09	0.000005	(serum transferrin)	0.43	[0.25-0.61] SD decrease	"Illumina [315,887]"	N
1/14/2009	19074352	Pollin	17-Dec-08	Science	http://www.ncbi.nlm.nih.gov/pubmed/19074352?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection	Triglycerides	809 individuals	698 individuals	11q23.3	"APOA1, APOC3, APOA4, APOA5, DSCAML1"	rs10892151-A	rs10892151	0.028	3.00E-29		NR	NR	"Affymetrix [381,934]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	6q25.1	ESR1	rs1038304-G	rs1038304	0.47	4.00E-10		0.08	[0.06-0.11] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	1p36.12	Intergenic	rs7524102-A	rs7524102	0.82	1.00E-16		0.15	[0.11-0.18] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	2q12.1	NR	rs6735786-C	rs6735786	0.64	0.000002		0.07	[0.04-0.09] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	17q21.31	SOST	rs1513670-A	rs1513670	0.37	2.00E-08		0.08	[0.05-0.10] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	Xq21.2	NR	rs2710057-T	rs2710057	0.67	0.000001		0.07	[0.04-0.09] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	17q21.31	C17orf53	rs227584-T	rs227584	0.73	9.00E-07		0.07	[0.04-0.10] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	3p22.1	NR	rs10490823-G	rs10490823	0.46	0.000009		0.06	[0.03-0.09] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (hip)	"6,865 individuals"	"8,510 individuals"	11p11.2	LRP4	rs1007738-A	rs1007738	0.77	7.00E-07		0.08	[0.05-0.11] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	21q11.2	NR	rs1006899-A	rs1006899	0.84	0.000006		0.09	[0.05-0.13] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	2p22.2	LOC344382	rs4670779-T	rs4670779	0.32	0.000004		0.07	[0.04-0.10] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	1p36.12	Intergenic	rs6696981-G	rs6696981	0.86	2.00E-08		0.12	[0.08-0.16] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	2p16.2	SPTBN1	rs11898505-G	rs11898505	0.68	0.000004		0.07	[0.04-0.10] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	6q25.1	"C6orf97, ESR1"	rs6929137-A	rs6929137	0.3	2.00E-10		0.1	[0.07-0.13] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	12q13.13	OSX	rs10876432-A	rs10876432	0.73	1.00E-07		0.08	[0.05-0.11] SD decrease	"Illumina [305,051]"	N
1/16/2009	19079262	Styrkarsdottir	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	New sequence variants associated with bone mineral density	Bone mineral density (spine)	"6,865 individuals"	"8,510 individuals"	13q14.11	RANKL	rs9594759-T	rs9594759	0.62	2.00E-17		0.12	[0.09-0.15] SD decrease	"Illumina [305,051]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	1p21.3	NR	rs10783050-C	rs10783050	0.36	0.000004		2.6	[1.50-3.70] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	19q13.11	"KCTD15, CHST8"	rs29941-C	rs29941	0.69	7.00E-12		4.18	[2.98-5.38] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	18q21.32	MC4R	rs12970134-A	rs12970134	0.3	1.00E-12		4.38	[3.16-5.60] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	16q12.2	FTO	rs8050136-A	rs8050136	0.41	1.00E-47		8.04	[6.96-9.12] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs925946-T	rs925946	0.34	9.00E-10		3.85	[2.62-5.08] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs7481311-T	rs7481311	0.24	0.000008		3.15	[1.78-4.52] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	3q27.2	"SFRS10, ETV5, DGKG"	rs7647305-C	rs7647305	0.77	7.00E-11		4.42	[3.09-5.75] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	2p25.3	TMEM18	rs7561317-G	rs7561317	0.84	4.00E-17		6.12	[4.69-7.55] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	1p31.1	NEGR1	rs2568958-A	rs2568958	0.58	1.00E-11		3.77	[2.67-4.87] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	16q12.2	FTO	rs6499640-A	rs6499640	0.41	4.00E-13		5.25	[3.82-6.68] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	16p11.2	"SH2B1, ATP2A1"	rs7498665-G	rs7498665	0.44	3.00E-10		3.63	[2.49-4.77] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	12q13.13	"BCDIN3D, FAIM2"	rs7138803-A	rs7138803	0.37	1.00E-07		3.28	[2.06-4.50] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs6265-G	rs6265	0.85	5.00E-10		4.58	[3.07-6.09] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Body mass index	"80,969 individuals"	"11,036 individuals"	1q25.2	"SEC16B, RASAL2"	rs10913469-C	rs10913469	0.2	6.00E-08		3.36	[2.14-4.58] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	1p31.1	NEGR1	rs2568958-A	rs2568958	0.58	2.00E-08		3.37	[2.19-4.55] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	1p21.3	NR	rs1973993-C	rs1973993	0.63	0.000001		2.71	[1.61-3.81] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	5q23.2	NR	rs2115172-A	rs2115172	0.57	0.000002		2.71	[1.59-3.83] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	16q12.2	FTO	rs6499640-A	rs6499640	0.65	6.00E-14		5.5	[4.07-6.93] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	19q13.11	"KCTD15, CHST8"	rs29941-C	rs29941	0.69	5.00E-09		3.73	[2.48-4.98] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	18q21.32	MC4R	rs12970134-A	rs12970134	0.3	5.00E-13		4.66	[3.41-5.91] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	16q12.2	FTO	rs8050136-A	rs8050136	0.41	5.00E-36		7.05	[5.95-8.15] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs7481311-T	rs7481311	0.24	0.000003		3.5	[2.03-4.97] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	1q25.2	"SEC16B, RASAL2"	rs10913469-C	rs10913469	0.2	1.00E-08		3.82	[2.51-5.13] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	16p11.2	"SH2B1, ATP2A1"	rs7498665-G	rs7498665	0.44	1.00E-09		3.69	[2.51-4.87] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	13q12.2	NR	rs7336332-G	rs7336332	0.15	0.000001		4.01	[2.40-5.62] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	12q13.13	"BCDIN3D, FAIM2"	rs7138803-A	rs7138803	0.37	2.00E-07		3.27	[2.05-4.49] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs6265-G	rs6265	0.85	2.00E-07		4	[2.47-5.53] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	11p14.1	BDNF	rs925946-T	rs925946	0.34	4.00E-09		3.8	[2.55-5.05] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	2p25.3	TMEM18	rs7561317-G	rs7561317	0.84	2.00E-18		6.47	[5.02-7.92] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	3q27.2	"SFRS10, ETV5, DGKG"	rs7647305-C	rs7647305	0.77	4.00E-09		4	[2.67-5.33] % SD	"Illumina [305,846]"	N
1/15/2009	19079260	Thorleifsson	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity	Weight	"80,969 individuals"	"11,036 individuals"	6p21.33	"AIF1, NCR3"	rs2844479-T	rs2844479	0.68	2.00E-08		3.58	[2.33-4.83] % SD	"Illumina [305,846]"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	4p13	GNPDA2	rs10938397-G	rs10938397	0.45	3.00E-16		0.19	[0.13-0.25] kg/m2	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	18q21.32	MC4R	rs17782313-C	rs17782313	0.21	5.00E-18		0.2	[0.12-0.28] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	2p25.3	TMEM18	rs6548238-C	rs6548238	0.84	1.00E-18		0.26	[0.19-0.34] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	16q12.2	FTO	rs9939609-A	rs9939609	0.41	4.00E-51		0.33	[0.27-0.39] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	11p11.2	MTCH2	rs10838738-G	rs10838738	0.34	5.00E-09		0.07	[0.01-0.13] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	19q13.11	KCTD15	rs11084753-G	rs11084753	0.67	2.00E-08		0.06	[-0.01-0.13] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	15q25.2	RKHD3	rs12324805-C	rs12324805	0.31	0.000007		NR	NR	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	20p12.3	BMP2	rs2145270-T	rs2145270	0.65	0.000006		NR	NR	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	11p15.4	STK33	rs10769908-C	rs10769908	0.53	0.000001		NR	NR	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	1p31.1	NEGR1	rs2815752-A	rs2815752	0.62	6.00E-08		0.1	[0.04-0.16] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
1/12/2009	19079261	Willer	14-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Six new loci associated with body mass index highlight a neuronal influence on body weight regulation	Body mass index	"32,387 individuals"	"59,092 individuals"	16p11.2	SH2B1	rs7498665-G	rs7498665	0.41	5.00E-11		0.15	[0.08-0.21] kg/m2 increase	"Illumina and Affymetrix [2,399,588] (imputed)"	N
2/5/2009	19081515	Mead	11-Dec-08	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/19081515?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study	Creutzfeldt-Jakob disease	"117 CJD cases, 3,083 controls"	"506 sCJD cases, 28 iCJD cases, 151 Kuru cases, 125 Kuru-resistant cases, up to 1,137 controls"	8q21.13	STMN2	rs1460163-A	rs1460163	NR	6.00E-08		NR	NR	"Affymetrix [288,908]"	N
2/5/2009	19081515	Mead	11-Dec-08	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/19081515?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study	Creutzfeldt-Jakob disease	"117 CJD cases, 3,083 controls"	"506 sCJD cases, 28 iCJD cases, 151 Kuru cases, 125 Kuru-resistant cases, up to 1,137 controls"	20p13	PRNP	rs1799990-A	rs1799990	NR	2.00E-21		NR	NR	"Affymetrix [288,908]"	N
1/6/2009	19065144	Sullivan	9-Dec-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/19065144?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo	Major depressive disorder	"1,738 cases, 1,802 controls"	"6,079 cases, 5,893 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Perlegen [435,291]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	19q13.32	"TOMM40, APOE"	rs2075650-G	rs2075650	0.15	3.00E-19		0.14	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	2p21	ABCG5	rs6756629-G	rs6756629	0.92	2.00E-11		0.15	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	1p36.11	TMEM57	rs10903129-G	rs10903129	0.54	5.00E-10		0.06	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	2p24.1	APOB	rs693-G	rs693	0.52	9.00E-23		0.1	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	11q12.2	"FADS2, FADS3"	rs174570-G	rs174570	0.83	2.00E-10		0.09	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	19p13.2	LDLR	rs2228671-G	rs2228671	0.88	9.00E-24		0.16	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	15q22.1	LIPC	rs1532085-G	rs1532085	0.59	4.00E-07		0.05	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	11q23.3	"APOA1, APOA4, APOA5, APOC3"	rs12272004-C	rs12272004	0.93	7.00E-07		0.11	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	8q24.13	TRIB1	rs6987702-G	rs6987702	0.29	3.00E-09		0.07	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	7p15.3	DNAH11	rs12670798-G	rs12670798	0.24	9.00E-07		0.06	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	5q13.3	HMGCR	rs3846662-G	rs3846662	0.44	3.00E-19		0.09	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	1p13.3	CELSR2	rs646776-G	rs646776	0.22	9.00E-22		0.13	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	18q21.1	LIPG	rs4939883-G	rs4939883	0.83	2.00E-11		0.07	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	19p13.11	NCAN	rs2304130-G	rs2304130	0.07	2.00E-15		0.15	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	"Cholesterol, total"	"22,562 individuals"	NR	1p31.3	DOCK7	rs10889353-C	rs10889353	0.32	4.00E-12		0.08	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	16q13	CETP	rs1532624-C	rs1532624	0.57	9.00E-94		0.21	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	2p24.1	APOB	rs6754295-C	rs6754295	0.25	4.00E-08		0.07	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	11p11.2	"MADD, FOLH1"	rs7395662-G	rs7395662	0.61	6.00E-11		0.07	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	8p21.3	LPL	rs2083637-G	rs2083637	0.26	6.00E-18		0.11	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	19q13.32	"TOMM40, APOE"	rs157580-G	rs157580	0.33	4.00E-07		0.06	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	9q31.1	ABCA1	rs3905000-G	rs3905000	0.86	9.00E-13		0.11	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	11q12.2	"FADS2, FADS3"	rs174570-G	rs174570	0.83	0.000004		0.06	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	15q22.1	LIPC	rs1532085-G	rs1532085	0.59	1.00E-35		0.13	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	18q21.1	LIPG	rs4939883-G	rs4939883	0.83	2.00E-11		0.1	[NR] SD increase	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	HDL cholesterol	"21,412 individuals"	NR	16q22.1	"CTCF, PRMT8"	rs2271293-G	rs2271293	0.87	8.00E-16		0.13	[NR] SD decrease	"Illumina and Affymetrix [up to ~600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	19q13.32	"TOMM40, APOE"	rs157580-G	rs157580	0.33	2.00E-19		0.11	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	11q12.2	"FADS2, FADS3"	rs174570-G	rs174570	0.83	4.00E-13		0.11	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	2p24.1	APOB	rs693-G	rs693	0.52	4.00E-17		0.1	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	1p31.3	DOCK7	rs10889353-C	rs10889353	0.32	0.000008		0.06	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	1p13.3	CELSR2	rs646776-G	rs646776	0.22	8.00E-23		0.16	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	5q13.3	HMGCR	rs3846662-G	rs3846662	0.44	2.00E-11		0.08	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	8q24.13	TRIB1	rs6987702-G	rs6987702	0.29	0.000003		0.07	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	11q23.3	"APOA1, APOA4, APOA5, APOC3"	rs12272004-C	rs12272004	0.93	5.00E-13		0.18	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	2p21	ABCG5	rs6756629-G	rs6756629	0.92	3.00E-10		0.16	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	7p15.3	DNAH11	rs12670798-G	rs12670798	0.24	6.00E-09		0.09	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	19p13.2	LDLR	rs2228671-G	rs2228671	0.88	4.00E-14		0.14	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	LDL cholesterol	"17,797 individuals"	NR	19p13.11	NCAN	rs2304130-G	rs2304130	0.07	0.000003		0.12	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	8p21.3	LPL	rs10096633-G	rs10096633	0.88	2.00E-18		0.17	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	2p23.3	GCKR	rs780094-G	rs780094	0.63	3.00E-20		0.1	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	2p24.1	APOB	rs6754295-C	rs6754295	0.25	3.00E-08		0.08	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	1p31.3	DOCK7	rs1167998-C	rs1167998	0.32	2.00E-12		0.09	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	11q23.3	"APOA1, APOA4, APOA5, APOC3"	rs12272004-C	rs12272004	0.93	5.00E-13		0.18	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	19p13.11	NCAN	rs2304130-G	rs2304130	0.07	0.000003		0.1	[NR] SD decrease	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	7q11.23	MLXIPL	rs2240466-G	rs2240466	0.87	1.00E-12		0.14	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/12/2009	19060911	Aulchenko	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts	Triglycerides	"17,815 individuals"	NR	19q13.32	"TOMM40, APOE"	rs439401-G	rs439401	0.68	2.00E-09		0.09	[NR] SD increase	"Illumina and Affymetrix [up to 600,000]"	N
1/7/2009	19060909	Bouatia-Naji	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk	Fasting plasma glucose	"2,151 individuals"	"6,332 cases, 9,132 controls"	11q21	MTNR1B	rs1387153-T	rs1387153	0.29	2.00E-36		0.07	[0.05-0.08] mmol/l increase	"Illumina [308,846]"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	9q31.1	ABCA1	rs1883025-T	rs1883025	0.26	1.00E-09		0.08	[0.04-0.12] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	1q42.13	GALNT2	rs4846914-G	rs4846914	0.4	4.00E-08		0.05	[0.01-0.09] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	16q22.1	LCAT	rs2271293-A	rs2271293	0.11	9.00E-13		0.07	[0.01-0.13] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	16q13	CETP	rs173539-T	rs173539	0.32	4.00E-75		0.25	[0.21-0.29] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	8p21.3	LPL	rs12678919-G	rs12678919	0.1	2.00E-34		0.23	[0.17-0.29] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	15q22.1	LIPC	rs10468017-T	rs10468017	0.3	8.00E-23		0.1	[0.06-0.14] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	18q21.1	LIPG	rs4939883-T	rs4939883	0.17	7.00E-15		0.14	[0.10-0.18] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	11q23.3	"APOA1, APOC3, APOA4, APOA5"	rs964184-G	rs964184	0.14	1.00E-12		0.17	[0.11-0.23] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	12q24.11	"MMAB,MVK"	rs2338104-C	rs2338104	0.45	1.00E-10		0.07	[0.03-0.11] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	11q12.2	"FADS1, FADS2, FADS3"	rs174547-C	rs174547	0.33	2.00E-12		0.09	[0.05-0.13] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	9p22.3	TTC39B	rs471364-C	rs471364	0.12	3.00E-10		0.08	[0.02-0.14] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	20q13.2	HNF4A	rs1800961-T	rs1800961	0.03	8.00E-10		0.19	[0.09-0.29] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	20q13.12	PLTP	rs7679-C	rs7679	0.19	4.00E-09		0.07	[0.03-0.11] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	HDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	19p13.2	ANGPTL4	rs2967605-T	rs2967605	0.16	1.00E-08		0.12	[0.04-0.20] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	5q13.3	HMGCR	rs3846663-T	rs3846663	0.38	8.00E-12		0.07	[0.03-0.11] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	19p13.11	"NCAN, CILP2, PBX4"	rs10401969-C	rs10401969	0.06	2.00E-08		0.05	[-0.03-0.13] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	19p13.2	LDLR	rs6511720-T	rs6511720	0.1	2.00E-26		0.26	[0.18-0.34] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	19q13.32	"APOE, APOC1, APOC4, APOC2"	rs4420638-G	rs4420638	0.16	4.00E-27		0.29	[0.17-0.41] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	2p24.1	APOB	rs515135-T	rs515135	0.2	5.00E-29		0.16	[0.12-0.20] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	12q24.31	HNF1A	rs2650000-A	rs2650000	0.36	2.00E-08		0.07	[0.03-0.11] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	1p13.3	"CELSR2, PSRC1, SORT1"	rs12740374-T	rs12740374	0.21	2.00E-42		0.23	[0.19-0.27] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	2p21	ABCG8	rs6544713-T	rs6544713	0.32	2.00E-20		0.15	[0.11-0.19] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	5q33.3	"TIMD4, HAVCR1"	rs1501908-G	rs1501908	0.37	1.00E-11		0.07	[0.03-0.11] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	20q12	MAFB	rs6102059-T	rs6102059	0.32	4.00E-09		0.06	[0.03-0.10] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	LDL cholesterol	"19,840 individuals"	"Up to 20,623 individuals"	1p32.3	PCSK9	rs11206510-C	rs11206510	0.19	4.00E-08		0.09	[0.05-0.13] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	8p23.1	"XKR6, AMAC1L2"	rs7819412-G	rs7819412	0.48	3.00E-08		0.04	[0.001-0.08] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	11q12.2	"FADS1, FADS2, FADS3"	rs174547-C	rs174547	0.33	2.00E-14		0.06	[0.02-0.10] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	1p31.3	ANGPTL3	rs10889353-C	rs10889353	0.33	3.00E-07		0.05	[0.01-0.09] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	20q13.12	PLTP	rs7679-C	rs7679	0.19	7.00E-11		0.07	[0.03-0.11] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	19p13.11	"NCAN,CILP2,PBX4"	rs17216525-T	rs17216525	0.07	4.00E-11		0.11	[0.05-0.17] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	7q11.23	MLXIPL	rs714052-G	rs714052	0.12	3.00E-15		0.16	[0.10-0.22] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	8q24.13	TRIB1	rs2954029-T	rs2954029	0.44	3.00E-19		0.11	[0.07-0.15] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	2p23.3	GCKR	rs1260326-T	rs1260326	0.45	2.00E-31		0.12	[0.08-0.16] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	8p21.3	LPL	rs12678919-G	rs12678919	0.1	2.00E-41		0.25	[0.19-0.31] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	11q23.3	"APOA1, APOC3, APOA4, APOA5"	rs964184-G	rs964184	0.14	4.00E-62		0.3	[0.24-0.36] SD increase	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060906	Kathiresan	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at 30 loci contribute to polygenic dyslipidemia	Triglycerides	"19,840 individuals"	"Up to 20,623 individuals"	2p24.1	APOB	rs7557067-G	rs7557067	0.22	9.00E-12		0.08	[0.04-0.12] SD decrease	"Affymetrix and Illumina [~2,600,000] (imputed)"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	HDL cholesterol	"4,763 individuals"	NR	11p11.2	NR1H3	rs7120118-G	rs7120118	0.42	4.00E-08		0.04	[0.03-0.05] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	HDL cholesterol	"4,763 individuals"	NR	16q22.1	LCAT	rs255049-G	rs255049	0.22	3.00E-08		0.05	[0.03-0.07] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	HDL cholesterol	"4,763 individuals"	NR	17p13.3	Intergenic	rs9891572-A	rs9891572	0.16	2.00E-07		0.05	[0.048-0.051] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	HDL cholesterol	"4,763 individuals"	NR	16q13	CETP	rs3764261-A	rs3764261	0.28	7.00E-29		0.09	[0.08-0.11] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	HDL cholesterol	"4,763 individuals"	NR	15q22.1	LIPC	rs1532085-A	rs1532085	0.44	2.00E-10		0.05	[0.03-0.06] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	1q32.2	CR1L	rs4844614-A	rs4844614	0.32	2.00E-07		0.1	[0.06-0.14] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	1p13.3	"CELSR2, PSRC1, SORT1"	rs646776-G	rs646776	0.21	2.00E-12		0.16	[0.11-0.20] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	19q13.32	APO cluster	rs157580-G	rs157580	0.29	5.00E-08		0.11	[0.07-0.15] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	19p13.2	LDLR	rs11668477-G	rs11668477	0.18	2.00E-07		0.13	[0.08-0.17] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	11q12.2	"FADS1, FADS2"	rs174546-A	rs174546	0.44	1.00E-07		0.1	[0.06-0.13] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	2p24.1	APOB	rs693-A	rs693	0.41	3.00E-11		0.12	[0.09-0.16] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	LDL cholesterol	"4,763 individuals"	NR	Xq12	AR	rs5031002-A	rs5031002	0.02	2.00E-07		0.3	[0.18-0.41] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	10q23.31	PANK1	rs11185790-A	rs11185790	0.21	3.00E-07	(INS)	0.31	[0.18-0.44] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	11q21	MTNR1B	rs1447352-G	rs1447352	0.42	6.00E-08	(GLU)	0.05	[0.03-0.06] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	2p24.1	APOB	rs673548-A	rs673548	0.27	2.00E-08	(TG)	0.08	[0.05-0.11] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	2p23.3	GCKR	rs1260326-A	rs1260326	0.35	4.00E-10	(TG)	0.09	[0.06-0.12] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	8p21.3	LPL	rs10096633-A	rs10096633	0.098	5.00E-08	(TG)	0.12	[0.07-0.17] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	15q14	Intergenic	rs2624265-G	rs2624265	0.42	4.00E-07	(TG)	0.07	[0.04-0.10] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	12q24.31	LEF1	rs2650000-A	rs2650000	0.45	3.00E-11	(CRP)	0.4	[0.25-0.55] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	2q24.3	"G6PC2, ABCB11"	rs560887-A	rs560887	0.31	6.00E-10	(GLU)	0.06	[0.04-0.07] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	7p21.2	Intergenic	rs10244051-C	rs10244051	0.46	1.00E-07	(GLU)	0.05	[0.03-0.06] mmol/l increase	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	1q23.2	CRP	rs2794520-A	rs2794520	0.36	3.00E-22	(CRP)	0.47	[0.32-0.62] mmol/l decrease	"Illumina [329,091]"	N
1/12/2009	19060910	Sabatti	7-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of metabolic traits in a birth cohort from a founder population	Other metabolic traits	"4,763 individuals"	NR	1p31.3	LEPR	rs12753193-G	rs12753193	0.45	4.00E-07	(CRP)	0.13	[-0.02-0.27] mmol/l decrease	"Illumina [329,091]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	14q23.2	Intergenic	rs1514928-?	rs1514928	NR	0.000003	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	16q22.1	HAS3	rs8047014-?	rs8047014	NR	0.000004	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	19q13.43	ZNF544	rs260461-?	rs260461	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	22q12.3	Intergenic	rs130575-?	rs130575	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	2q14.3	Intergenic	rs17367118-?	rs17367118	NR	0.000009	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	2q24.1	Intergenic	rs1918172-?	rs1918172	NR	0.000005	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	3p24.3	Intergenic	rs11719664-?	rs11719664	NR	0.000002	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	8q24.3	NAPRT1	rs2290416-?	rs2290416	NR	0.000009	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	4q13.3	EREG	rs1350666-?	rs1350666	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	1q41	Intergenic	rs1018040-?	rs1018040	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	3p14.1	FOXP1	rs17651978-?	rs17651978	NR	0.000006	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	2q21.2	FLJ34870	rs7577925-?	rs7577925	NR	0.000003	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	12p11.22	Intergenic	rs522958-?	rs522958	NR	0.000001	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	2q14.1	Intergenic	rs272000-?	rs272000	NR	0.000009	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	3p14.2	FHIT	rs6791644-?	rs6791644	NR	0.000008	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	2p21	OXER1	rs930421-?	rs930421	NR	0.000006	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	1p31.2	Intergenic	rs4147141-?	rs4147141	NR	0.000006	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	11p13	Intergenic	rs10767942-?	rs10767942	NR	0.000008	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Attention deficit hyperactivity disorder	909 trios	NR	13q32.3	CLYBL	rs7992643-?	rs7992643	NR	0.000005	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	14q23.1	Intergenic	rs1335515-C	rs1335515	NR	0.000008	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	20q13.13	SULF2	rs4810685-C	rs4810685	NR	0.000007	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	7q31.1	Intergenic	rs6968385-T	rs6968385	NR	0.000002	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	11p15.1	Intergenic	rs874426-C	rs874426	NR	0.000004	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	2q36.3	Intergenic	rs1517484-C	rs1517484	NR	5.00E-07	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	3p22.3	Intergenic	rs9845475-G	rs9845475	NR	0.000004	(later onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	3q29	Intergenic	rs3892715-C	rs3892715	NR	0.000006	(earlier onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	5q35.3	ADAMTS2	rs10039254-A	rs10039254	NR	0.000008	(later onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	6q15	Intergenic	rs806276-A	rs806276	NR	3.00E-07	(later onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	8q23.3	Intergenic	rs17658378-A	rs17658378	NR	0.000009	(later onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18937294	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder (time to onset)	930 trios	NR	9p23	Intergenic	rs1325154-C	rs1325154	NR	0.000005	(later onset)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	6p22.3	Intergenic	rs1202199-?	rs1202199	NR	0.000009	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	6p22.3	Intergenic	rs41441749-?	rs41441749	NR	0.000001	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	21q21.3	GRIK1	rs363512-?	rs363512	NR	0.000004	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	9p24.3	DMRT2	rs17641078-?	rs17641078	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	3q26.1	Intergenic	rs6808138-?	"rs6808138,rs6808138"	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	2p21	OXER1	rs6719977-?	rs6719977	NR	0.000002	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	18q22.1	Intergenic	rs13353224-?	rs13353224	NR	0.000009	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	3q26.1	Intergenic	rs6808138-?	rs6808138	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	8p21.3	LPL	rs7816032-?	rs7816032	NR	0.000002	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	12p11.22	Intergenic	rs522958-?	rs522958	NR	8.00E-07	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	1q41	Intergenic	rs1018040-?	rs1018040	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	1p13.2	Intergenic	rs11590090-?	rs11590090	NR	0.000003	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	19q13.43	LOC390980	rs2014572-?	rs2014572	NR	0.000007	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Hyperactive-impulsive symptoms	909 trios	NR	15q14	MEIS2	rs8041675-?	rs8041675	NR	0.000004	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	9q21.31	Intergenic	rs2769967-?	rs2769967	NR	0.000003	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	7q36.3	Intergenic	rs10227331-?	rs10227331	NR	0.000004	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	16q23.1	Intergenic	rs13330107-?	rs13330107	NR	0.000009	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	16q12.1	ZNF423	rs17281813-?	rs17281813	NR	0.000003	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	15q26.1	SLCO3A1	rs7495052-?	rs7495052	NR	0.000003	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	11q22.3	Intergenic	rs10895959-?	rs10895959	NR	0.000003	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	8q21.11	Intergenic	rs12679254-?	rs12679254	NR	0.000002	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	15q13.1	Intergenic	rs1471225-?	rs1471225	NR	0.000008	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	15q25.1	IL16	rs7172689-?	rs7172689	NR	0.000004	(count)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	12q24.22	Intergenic	rs478597-?	rs478597	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	13q12.12	Intergenic	rs17079773-?	rs17079773	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	8p11.21	Intergenic	rs11786458-?	rs11786458	NR	0.000009	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	1p31.2	Intergenic	rs4650135-?	rs4650135	NR	0.000005	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	9q22.32	Intergenic	rs11790994-?	rs11790994	NR	2.00E-07	(binary)	NR	NR	"Perlegen [429,981]"	N
5/7/2009	18821565	Lasky-Su	5-Dec-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations	Inattentive symptoms	909 trios	NR	1p31.2	Intergenic	rs4147141-?	rs4147141	NR	0.000008	(binary)	NR	NR	"Perlegen [429,981]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	11p15.1	KCNJ11	rs5219-?	rs5219	NR	1.00E-09	(non-obese)	1.25	[1.16-1.34]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	11p15.1	KCNJ11	rs5219-?	rs5219	NR	5.00E-07	(obese)	1.19	[1.11-1.27]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	16q12.2	FTO	rs8050136-?	rs8050136	NR	2.00E-17	(obese)	1.3	[1.23-1.39]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	8q24.11	SLC30A8	rs13266634-?	rs13266634	NR	0.000007	(non-obese)	1.18	[1.10-1.27]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	10q25.2	TCF7L2	rs7903146-?	rs7903146	NR	9.00E-30	(non-obese)	1.49	[1.39-1.59]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	9p21.3	CDKN2B	rs10811661-?	rs10811661	NR	7.00E-07	(non-obese)	1.26	[1.15-1.38]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	10q25.2	TCF7L2	rs7903146-?	rs7903146	NR	6.00E-16	(obese)	1.31	[1.23-1.40]	"Affymetrix [393,453]"	N
1/15/2009	19056611	Timpson	3-Dec-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls"	6p22.3	CDKAL	rs10946398-?	rs10946398	NR	7.00E-07	(non-obese)	1.18	[1.11-1.26]	"Affymetrix [393,453]"	N
1/12/2009	19047183	Friedman	1-Dec-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19047183?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	grm7 variants confer susceptibility to age-related hearing impairment	Hearing impairment	"846 cases, 846 controls"	"63 cases, 67 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [506,627] (pooled)"	N
2/26/2009	19060907	Prokopenko	1-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in MTNR1B influence fasting glucose levels	Fasting plasma glucose	"35,812 individuals"	NR	11q21	MTNR1B	rs10830963-G	rs10830963	0.28	3.00E-50		0.07	[0.06-0.08] mmol/l increase	"Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)"	N
2/26/2009	19060907	Prokopenko	1-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in MTNR1B influence fasting glucose levels	Fasting plasma glucose	"35,812 individuals"	NR	7p13	GCK	rs4607517-A	rs4607517	0.18	1.00E-25		0.06	[0.05-0.07] mmol/l increase	"Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)"	N
2/26/2009	19060907	Prokopenko	1-Dec-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in MTNR1B influence fasting glucose levels	Fasting plasma glucose	"35,812 individuals"	NR	2q24.3	G6PC2	rs560887-C	rs560887	0.7	1.00E-57		0.06	[0.05-0.07] mmol/l increase	"Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	12q24.21	Intergenic	rs2194980-?	rs2194980	0.33	3.00E-07	(Tyrosine)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	15q26.1	SV2B	rs886144-?	rs886144	0.38	2.00E-07	(SM)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	6q25.1	C6orf71	rs1591830-?	rs1591830	0.32	1.00E-07	(sugar)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	6q12	Intergenic	rs9354308-?	rs9354308	0.37	3.00E-07	(serotonin)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	3p25.3	ATP2B2	rs6807064-?	rs6807064	0.29	1.00E-07	(phenylalanine)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	6q26	PARK2	rs992037-?	rs992037	0.35	1.00E-07	(Lysine)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	2p14	PLEK	rs9309413-?	rs9309413	0.45	2.00E-09	(SM)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	11q12.2	FADS1	rs174548-?	rs174548	0.28	5.00E-08	(PC)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	15q22.1	LIPC	rs4775041-?	rs4775041	0.28	1.00E-07	(PE)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	3q22.3	Intergenic	rs1382269-?	rs1382269	0.47	5.00E-07	(SM)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	3q28	FGF12	rs4453795-?	rs4453795	0.41	4.00E-07	(PC)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	4q13.1	Intergenic	rs10517480-?	rs10517480	0.31	2.00E-07	(PC)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	7q31.1	Intergenic	rs10953730-?	rs10953730	0.35	2.00E-07	(acylcarnitine)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	16p13.2	A2BP1	rs9924951-?	rs9924951	0.41	5.00E-07	(PC)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	13q31.3	GPC5	rs17267292-?	rs17267292	0.28	1.00E-07	(Docosahexaonic acid)	NR	NR	"Affymetrix [187,454]"	N
12/24/2008	19043545	Gieger	28-Nov-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum	Serum metabolites	284 males	NR	10p11.21	ANKRD30A	rs1148259-?	rs1148259	0.42	3.00E-09	(SM)	NR	NR	"Affymetrix [187,454]"	N
12/9/2008	18957941	Terracciano	24-Nov-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for five major dimensions of personality	Personality dimensions	"3,972 individuals"	"3,903 individuals"	2p22.1	THUMPD2	rs2540226-T	rs2540226	0.53	0.000003	(agreeableness)	0.13	[NR] SD increase	"Affymetrix [362,129]"	N
12/9/2008	18957941	Terracciano	24-Nov-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for five major dimensions of personality	Personality dimensions	"3,972 individuals"	"3,903 individuals"	19q13.31	ZNF180	rs644148-G	rs644148	0.5	0.000008	(extraversion)	0.14	[NR] SD increase	"Affymetrix [362,129]"	N
12/9/2008	18957941	Terracciano	24-Nov-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for five major dimensions of personality	Personality dimensions	"3,972 individuals"	"3,903 individuals"	4q12	CLOCK	rs6832769-A	rs6832769	0.73	0.000002	(agreeableness)	0.14	[NR] SD decrease	"Affymetrix [362,129]"	N
12/9/2008	18957941	Terracciano	24-Nov-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for five major dimensions of personality	Personality dimensions	"3,972 individuals"	"3,903 individuals"	Xp11.3	FUNDC1	rs6610953-G	rs6610953	0.85	0.000006	(openness)	0.15	[NR] SD increase	"Affymetrix [362,129]"	N
12/9/2008	18957941	Terracciano	24-Nov-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for five major dimensions of personality	Personality dimensions	"3,972 individuals"	"3,903 individuals"	19q13.31	ZNF180	rs644148-G	rs644148	0.5	9.00E-07	(openness)	0.15	[NR] SD increase	"Affymetrix [362,129]"	N
1/7/2009	19030899	Lei	23-Nov-08	Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/19030899?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci	Height	618 Chinese individuals	"2,953 Chinese individuals"	9q22.23	ZNP510	rs10816533-C	rs10816533	0.29	0.000002		NR	NR	"Affymetrix [281,533]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	3p12.3	"ROBO2, ROBO1"	rs9836484-?	rs9836484	0.32	0.000004		NR	NR	"Illumina [302,783]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	6q16.2	POU3F2	rs9491640-?	rs9491640	0.06	0.000009		NR	NR	"Illumina [302,783]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	3q26.2	TNIK	rs2088885-?	rs2088885	0.47	0.000006		NR	NR	"Illumina [302,783]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	5q23.2	"CTXN3, SLC12A2"	rs245201-?	rs245201	0.32	9.00E-08		NR	NR	"Illumina [302,783]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	2q37.3	GPC1	rs1574192-?	rs1574192	0.38	0.000004		NR	NR	"Illumina [302,783]"	N
1/6/2009	19023125	Potkin	20-Nov-08	Schizophr Bull	http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype	Brain imaging in schizophrenia (interaction)	"64 cases, 74 cases"	NR	14q32.32	TRAF3	rs10133111-?	rs10133111	0.2	0.000005		NR	NR	"Illumina [302,783]"	N
12/1/2008	19011631	COGENT Study	16-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer	Colorectal cancer	"1,902 cases, 1,929 controls"	"4,878 cases, 4,914 controls"	19q13.11	RHPN2	rs10411210-C	rs10411210	0.9	5.00E-09		1.15	[1.10-1.20]	"Illumina [up to 548,586]"	N
12/1/2008	19011631	COGENT Study	16-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer	Colorectal cancer	"1,902 cases, 1,929 controls"	"4,878 cases, 4,914 controls"	14q22.2	BMP4	rs4444235-C	rs4444235	0.46	8.00E-10		1.11	[1.08-1.15]	"Illumina [up to 548,586]"	N
12/1/2008	19011631	COGENT Study	16-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer	Colorectal cancer	"1,902 cases, 1,929 controls"	"4,878 cases, 4,914 controls"	16q22.1	CDH1	rs9929218-A	rs9929218	0.29	1.00E-08		1.1	[1.06-1.12]	"Illumina [up to 548,586]"	N
12/1/2008	19011631	COGENT Study	16-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer	Colorectal cancer	"1,902 cases, 1,929 controls"	"4,878 cases, 4,914 controls"	20p12.3	Intergenic	rs961253-A	rs961253	0.36	2.00E-10		1.12	[1.08-1.16]	"Illumina [up to 548,586]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Brain lesion load	"791 cases, 883 controls"	NR	6q25.3	IGF2R	rs6917747-?	rs6917747	0.15	0.000007		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Brain lesion load	"791 cases, 883 controls"	NR	14q12	NUBPL	rs2039485-?	rs2039485	0.22	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Brain lesion load	"791 cases, 883 controls"	NR	19p13.11	CPAMD8	rs11666377-?	rs11666377	0.14	0.000007		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Brain lesion load	"791 cases, 883 controls"	NR	2q37.1	CHRND	rs2602397-?	rs2602397	0.45	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	3q23	SLC25A36	rs908821-?	rs908821	0.71	0.000003		1.37	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	2q14.2	EN1	rs651477-?	rs651477	0.26	0.000007		1.38	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	4q35.1	MGC45800	rs7672826-?	rs7672826	0.34	0.000008		1.37	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	3q24	ZIC1	rs1841770-?	rs1841770	0.53	0.000008		1.34	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	13q31.3	GPC5	rs9523762-?	rs9523762	0.35	0.000001		1.36	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	20p13	C20orf46	rs397020-?	rs397020	0.52	8.00E-07		1.41	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	8p23.2	CSMD1	rs1529316-?	rs1529316	0.47	0.000002		1.36	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	9p22.2	SH3GL2	rs1755289-?	rs1755289	0.61	0.000003		1.35	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	2p25.1	DDEF2	rs1109670-?	rs1109670	0.26	0.000009		1.38	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis	"978 cases, 883 controls"	NR	12q12	PDZRN4	rs1458175-?	rs1458175	0.49	0.000002		1.34	[NR]	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	18q21.31	WDR7	rs1557351-?	rs1557351	0.22	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	11q14.2	RAB38	rs1386330-?	rs1386330	0.13	0.000002		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	5q33.2	SGCD	rs4704970-?	rs4704970	0.2	0.000007		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	1q25.2	C1orf125	rs12047808-?	rs12047808	0.13	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	8q13.3	KCNB2	rs2116078-?	rs2116078	0.48	0.000003		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	7q22.1	RELN	rs17157903-?	rs17157903	0.14	0.000003		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	2q21.2	FLJ34870	rs1437898-?	rs1437898	0.4	0.000008		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (age of onset)	"978 cases, 883 controls"	NR	9q21.13	RFK	rs2842483-?	rs2842483	0.29	0.000005		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	6p23	JARID2	rs6941421-?	rs6941421	0.24	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	16q22.3	C16orf47	rs7191888-?	rs7191888	0.17	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	7q31.2	MET	rs10243024-?	rs10243024	0.23	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	11q23.3	MGC13125	rs180358-?	rs180358	0.23	0.000006		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	4q13.2	CENPC1	rs10518025-?	rs10518025	0.14	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	7p21.3	C1GALT1	rs10259085-?	rs10259085	0.46	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	19p13.2	ACP5	rs7253363-?	rs7253363	0.05	0.000009		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	18q22.3	CBLN2	rs337718-?	rs337718	0.29	0.000009		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	19q13.42	NLRP11	rs299175-?	rs299175	0.46	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	4q28.3	LOC132321	rs1478091-?	rs1478091	0.06	0.000002		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Multiple sclerosis (severity)	"794 cases, 883 controls"	NR	3q25.32	FLJ16641	rs12638253-?	rs12638253	0.47	0.000002		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Normalized brain volume	"753 cases, 883 controls"	NR	12p11.21	BICD1	rs261902-?	rs261902	0.16	0.000004		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Normalized brain volume	"753 cases, 883 controls"	NR	10p11.23	SVIL	rs1927457-?	rs1927457	0.31	0.000008		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Normalized brain volume	"753 cases, 883 controls"	NR	10q25.2	MXI1	rs716595-?	rs716595	0.08	0.000008		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Normalized brain volume	"753 cases, 883 controls"	NR	6q21	FOXO3	rs9480865-?	rs9480865	0.16	0.000007		NR	NR	"Illumina [551,642]"	N
1/16/2009	19010793	Baranzini	14-Nov-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis	Normalized brain volume	"753 cases, 883 controls"	NR	5q35.1	KCNIP1	rs11957313-?	rs11957313	0.13	0.000009		NR	NR	"Illumina [551,642]"	N
12/9/2008	18997785	Aulchenko	9-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18997785?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor	Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis	Multiple sclerosis	"45 cases, 195 controls"	"2,634 cases, 2,930 controls"	1p36.22	KIF1B	rs10492972-C	rs10492972	0.27	3.00E-10		1.34	[1.23-1.48]	"Affymetrix [~250,000]"	N
12/1/2008	18997786	Bilguvar	9-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Susceptibility loci for intracranial aneurysm in European and Japanese populations	Intracranial aneurysm	"1,580 European cases, 6,276 European controls"	"495 Japanese cases, 676 Japanese controls"	8q11.23	SOX17	rs10958409-A	rs10958409	0.15	1.00E-10		1.36	[1.24-1.49]	"Illumina [289,271]"	N
12/1/2008	18997786	Bilguvar	9-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Susceptibility loci for intracranial aneurysm in European and Japanese populations	Intracranial aneurysm	"1,580 European cases, 6,276 European controls"	"495 Japanese cases, 676 Japanese controls"	9q21.3	"CDKN2A, CDKN2B"	rs1333040-T	rs1333040	0.55	1.00E-10		1.29	[1.19-1.40]	"Illumina [289,271]"	N
12/1/2008	18997786	Bilguvar	9-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Susceptibility loci for intracranial aneurysm in European and Japanese populations	Intracranial aneurysm	"1,580 European cases, 6,276 European controls"	"495 Japanese cases, 676 Japanese controls"	8q11.23-q12.1	SOX17	rs9298506-A	rs9298506	0.81	2.00E-09		1.35	[1.22-1.49]	"Illumina [289,271]"	N
12/1/2008	18997786	Bilguvar	9-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Susceptibility loci for intracranial aneurysm in European and Japanese populations	Intracranial aneurysm	"1,580 European cases, 6,276 European controls"	"495 Japanese cases, 676 Japanese controls"	2q33.1	"BOLL, PLCL1"	rs700651-G	rs700651	0.35	4.00E-08		1.24	[1.15-1.34]	"Illumina [289,271]"	N
12/30/2008	19009022	Drgon	9-Nov-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/19009022?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome wide association for nicotine dependence and smoking cessation success in NIH research volunteers	Nicotine dependence	"220 cases, 260 controls"	"2,271 cases, 1,868 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~600,00] (pooled)"	N
12/9/2008	18985386	Pankratz	6-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18985386?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association study for susceptibility genes contributing to familial Parkinson disease	Parkinson's disease (familial)	"857 cases, 867 controls"	"262 cases, 260 controls"	4p16.3	"GAK, DGKQ"	rs1564282-T	rs1564282	0.09	7.00E-07		1.7	[NR]	"Illumina [328,189]"	N
12/9/2008	18987618	Cronin	5-Nov-08	Eur J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18987618?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSu	Screening for replication of genome-wide SNP associations in sporadic AL	Amyotrophic lateral sclerosis	"958 cases, 932 controls"	"309 cases, 404 controls"	7q36.2	DPP6	rs10260404-C	rs10260404	0.35	0.000003		1.37	[1.20-1.56]	"Illumina [287,522]"	N
12/1/2008	18980221	Neale	3-Nov-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18980221?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide association scan of attention deficit hyperactivity disorder	Attention deficit hyperactivity disorder	909 trios	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Perlegen [438,784]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	10p15.1	IL2RA	rs12251307-T	rs12251307	NR	0.000002		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	22q13.1	C1QTNF6	rs229541-T	rs229541	0.43	2.00E-08		1.04	[0.97-1.12]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	6p21.32	HLA	rs9272346-G	rs9272346	NR	6.00E-129		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	2q33.2	CTLA4	rs3087243-A	rs3087243	NR	8.00E-11		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	16p13.13	"C16orf75, PRM3, TNP2"	rs416603-T	rs416603	0.44	0.000003		1.06	[1.01-1.12]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	15q25.1	CTSH	rs3825932-C	rs3825932	0.32	3.00E-15		1.16	[1.10-1.22]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	10p15.1	PRKCQ	rs947474-G	rs947474	0.19	4.00E-09		1.1	[1.03-1.18]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	6q15	BACH2	rs11755527-G	rs11755527	0.47	5.00E-12		1.13	[1.08-1.19]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	2p23.3	Intergenic	rs2165738-C	rs2165738	0.27	0.000004		1.07	[1.01-1.13]	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	18p11.21	PTPN2	rs2542151-C	rs2542151	NR	9.00E-08		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	12q24.13	C12orf30	rs17696736-G	rs17696736	NR	6.00E-18		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	12q13.2	ERBB3	rs2292239-A	rs2292239	NR	3.00E-16		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	16p13.13	CLEC16A	rs12708716-G	rs12708716	NR	7.00E-13		NR	NR	"Affymetrix [up to 335,565]"	N
11/25/2008	18978792	Cooper	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci	Type 1 diabetes	"3,561 cases, 4,646 controls"	"6,225 cases, 6,946 controls, 3,064 trios"	1p13.2	PTPN22	rs6679677-A	rs6679677	NR	1.00E-40		NR	NR	"Affymetrix [up to 335,565]"	N
12/9/2008	18978790	McKay	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978790?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Lung cancer susceptibility locus at 5p15.33	Lung cancer	"2,971 cases, 3,746 controls"	"2,899 cases, 5,573 controls"	5p15.33	"TERT, CLPTM1"	rs402710-C	rs402710	NR	0.000004		1.18	[1.12-1.24]	"Illumina [315,194]"	N
12/9/2008	18978790	McKay	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978790?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Lung cancer susceptibility locus at 5p15.33	Lung cancer	"2,971 cases, 3,746 controls"	"2,899 cases, 5,573 controls"	15q25.1	Intergenic	rs1051730-A	rs1051730	NR	1.00E-15		1.35	[1.25-1.45]	"Illumina [315,194]"	N
11/25/2008	18978787	Wang	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common 5p15.33 and 6p21.33 variants influence lung cancer risk	Lung cancer	"1,952 cases, 1,438 controls"	"7,579 cases, 8,236 controls"	6p21.33	"BAT3,MSH5"	rs3117582-C	rs3117582	NR	5.00E-10		1.24	[1.16-1.33]	"Illumina [223,891]"	N
11/25/2008	18978787	Wang	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common 5p15.33 and 6p21.33 variants influence lung cancer risk	Lung cancer	"1,952 cases, 1,438 controls"	"7,579 cases, 8,236 controls"	5p15.33	CLPTM1L	rs401681-G	rs401681	NR	8.00E-09		1.15	[1.09-1.19]	"Illumina [223,891]"	N
11/25/2008	18978787	Wang	2-Nov-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common 5p15.33 and 6p21.33 variants influence lung cancer risk	Lung cancer	"1,952 cases, 1,438 controls"	"7,579 cases, 8,236 controls"	15q25.1	NR	rs8042374-?	rs8042374	NR	8.00E-12		NR	NR	"Illumina [223,891]"	N
12/9/2008	18976728	Bertram	29-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18976728?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE	Alzheimer's disease	"941 affected individuals, 404 unaffected individuals"	"1,767 affected individuals, 838 unaffected individuals"	14q31.2	Intergenic	rs11159647-?	rs11159647	NR	0.000002		NR	NR	"Affymetrix [484,522]"	N
12/9/2008	18976728	Bertram	29-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18976728?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE	Alzheimer's disease	"941 affected individuals, 404 unaffected individuals"	"1,767 affected individuals, 838 unaffected individuals"	19q13.33	CD33	rs3826656-?	rs3826656	NR	0.000006		NR	NR	"Affymetrix [484,522]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	7q31.1	"FLJ31818, GPR85"	rs10229603-C	rs10229603	0.31	0.000005		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	12q21.2	PAWR	rs7297018-A	rs7297018	0.19	0.000004		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	13q12.2	"GSX1, PDX1"	rs9512900-C	rs9512900	0.37	0.000009		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	13q33.3	"LIG4, ABHD13"	rs10492664-C	rs10492664	0.84	0.000001		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	1q42.13	LOC729257	rs701157-C	rs701157	0.45	0.000004		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	16q21	Intergenic	rs1381102-A	rs1381102	0.4	0.000006		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	1q25.3	"RGL1, GLT25D2"	rs10797919-G	rs10797919	0.59	0.000009		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	10p14	A2BP1	rs1291846-T	rs1291846	0.19	0.000009		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	15q26.2	SPATA8	rs4533251-T	rs4533251	0.15	0.000004		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	11q24.2	KIRREL3	rs1557488-T	rs1557488	0.18	0.000005		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	14q12	Intergenic	rs1951082-T	rs1951082	0.43	0.000005		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	12q15	C12orf28	rs789560-G	rs789560	0.87	0.000007		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	4q13.3	"AMOTL1, CWC15, JMJD2D"	rs10831284-G	rs10831284	0.13	0.000002		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	18q21.31	ATP8B1	rs7236632-A	rs7236632	0.86	0.000006		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	16q22.3	"PKD1L3, KIAA0174, DHODH"	rs16973500-C	rs16973500	0.86	0.000007		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	16q23.2	"PKD1L2, C16orf46"	rs4889240-T	rs4889240	0.45	0.000007		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	21q21.1	Intergenic	rs2826340-T	rs2826340	0.17	0.000002		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	1p35.2	Intergenic	rs2180233-C	rs2180233	0.31	0.000009		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	1q23.1	"ETV3L, ETV3"	rs6427356-G	rs6427356	0.28	0.000008		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	2p22.3	Intergenic	rs6733379-G	rs6733379	0.28	0.000004		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	2p12	Intergenic	rs7595103-A	rs7595103	0.64	0.000007		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	2q33.1	"FLJ39061, FZD7"	rs1521882-A	rs1521882	0.82	0.000008		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	5q31.1	C5orf15	rs1644305-A	rs1644305	0.41	0.000008		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	8q22.3	YWHAZ	rs931812-C	rs931812	0.74	0.000005		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	9p24.1	PTPRD	rs10815798-A	rs10815798	0.48	0.000006		NR	NR	"Perlegen [378,332]"	N
12/9/2008	18951430	Anney	24-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study	Attention deficit hyperactivity disorder and conduct disorder	938 affected trios	NR	10p15.2	PITRM1	rs2764980-A	rs2764980	0.51	0.000009		NR	NR	"Perlegen [378,332]"	N
12/1/2008	18952825	Johansson	24-Oct-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/18952825?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis	Height	"3,925 individuals"	"38,091 individuals"	7p15.1	JAZF1	rs1635852-A	rs1635852	NR	9.00E-10		0.25	[0.17-0.33] cm taller	Illumina [NR]	N
12/9/2008	18941528	Comabella	22-Oct-08	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/18941528?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms"	Multiple sclerosis	"242 cases, 242 controls"	"375 cases, 375 controls"	6p21.32	HLA-DRB1	rs3129934-T	rs3129934	NR	9.00E-11		3.3	[2.3-4.9]	"Affymetrix [428,867] (pooled)"	N
11/25/2008	18849994	Hillmer	12-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18849994?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Susceptibility variants for male-pattern baldness on chromosome 20p11	Male-pattern baldness	"296 cases, 347 controls"	"319 cases, 234 controls"	20p11.22	"PAX1, BQ013595, BE789145"	rs2180439-C	rs2180439	0.43	3.00E-15		1.82	[1.45-2.30]	"Illumina [531,695]"	N
11/25/2008	18849991	Richards	12-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18849991?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Male-pattern baldness susceptibility locus at 20p11	Male-pattern baldness	"578 cases, 547 controls"	"1,351 cases, 2,485 controls"	Xq12	AR	rs6625163-A	rs6625163	NR	5.00E-11		3.3	[2.31-4.71]	"Affymetrix [370,102]"	N
11/25/2008	18849991	Richards	12-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18849991?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Male-pattern baldness susceptibility locus at 20p11	Male-pattern baldness	"578 cases, 547 controls"	"1,351 cases, 2,485 controls"	20p11.22	PAX1	rs1160312-A	rs1160312	0.43	1.00E-14	(males)	1.6	[1.42-1.80] (males)	"Affymetrix [370,102]"	N
11/25/2008	18849993	Stacey	12-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18849993?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits	Basal cell carcinoma (cutaneous)	"930 cases, 33,117 controls"	"1,216 cases, 2,844 controls"	1q42.13	RHOU	rs801114-G	rs801114	0.33	6.00E-12		1.28	[1.19-1.37]	"Illumina [304,083]"	N
11/25/2008	18849993	Stacey	12-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18849993?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits	Basal cell carcinoma (cutaneous)	"930 cases, 33,117 controls"	"1,216 cases, 2,844 controls"	1p36.13	"PADI4, PADI6,RCC2, ARHGEF10L"	rs7538876-A	rs7538876	0.35	4.00E-12		1.28	[1.19-1.37]	"Illumina [304,083]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	10q21.3	POU2F1	rs9803659-C	rs9803659	NR	0.000004	(ALT)	0.03	[0.018-0.042] U/L decrease	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	9q34.2	ADAMTS13	rs4962153-A	rs4962153	NR	8.00E-21	(ALP)	0.06	[0.048-0.072] U/L decrease	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	22q13.31	"PNPLA3, SAMM50"	rs2281135-T	rs2281135	0.18	8.00E-16	(ALT)	0.06	[0.046-0.074] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	6p22.2	GPLD1	rs9467160-A	rs9467160	0.24	1.00E-11	(ALP)	0.03	[0.024-0.044] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	10q24.31	JMJD1C	rs12355784-A	rs12355784	0.48	5.00E-10	(ALP)	0.03	[0.017-0.033] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	1p36.12	"NBPF3, ALPL, RAP1GAP"	rs1780324-T	rs1780324	0.43	7.00E-15	(ALP)	0.03	[0.023-0.039] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	9p34.2	ABO	rs657152-T	rs657152	0.39	2.00E-30	(ALP)	0.05	[0.039-0.055] U/L decrease	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	22q11.23	"GGT1, C22orf36"	rs4820599-G	rs4820599	0.31	4.00E-11	(GGT)	0.01	[0.005-0.009] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	10q24.2q	"CPN1, CHUK, ERLIN1"	rs11597390-A	rs11597390	0.36	2.00E-08	(ALT)	0.04	[0.025-0.053] U/L decrease	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	12q24.2	"HNF1A, C12orf27, C12orf43"	rs1169313-C	rs1169313	0.38	2.00E-10	(GGT)	0.01	[0.003-0.007] U/L decrease	"Affymetrix and Illumina [up to 496,032]"	N
12/1/2008	18940312	Yuan	10-Oct-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes	Plasma levels of liver enzymes	"7,751 European white individuals"	"4,704 European white and Indian Asian individua"	10q21.2	REEP3	rs10761779-G	rs10761779	0.49	7.00E-10	(ALP)	0.03	[0.017-0.033] U/L increase	"Affymetrix and Illumina [up to 496,032]"	N
11/25/2008	18840781	Grant	7-Oct-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes	Type 1 diabetes	"563 cases, 1,146 controls, 483 case-parents trios"	"636 families, 3,303 cases, 4,673 controls"	6q15	BACH2	rs3757247-A	rs3757247	NR	1.00E-06		1.13	[1.08-1.19]	"Illumina [up to 1,000,000]"	N
11/25/2008	18840781	Grant	7-Oct-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes	Type 1 diabetes	"563 cases, 1,146 controls, 483 case-parents trios"	"636 families, 3,303 cases, 4,673 controls"	9p24.2	GLIS3	rs10758593-A	rs10758593	NR	0.000003		1.13	[1.07-1.19]	"Illumina [up to 1,000,000]"	N
11/25/2008	18840781	Grant	7-Oct-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes	Type 1 diabetes	"563 cases, 1,146 controls, 483 case-parents trios"	"636 families, 3,303 cases, 4,673 controls"	15q14	RASGRP1	rs8035957-C	rs8035957	NR	4E-06		1.14	[1.08-1.21]	"Illumina [up to 1,000,000]"	N
11/25/2008	18840781	Grant	7-Oct-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes	Type 1 diabetes	"563 cases, 1,146 controls, 483 case-parents trios"	"636 families, 3,303 cases, 4,673 controls"	21q22.3	UBASH3A	rs9976767-C	rs9976767	NR	2.00E-08		1.16	[1.10-1.22]	"Illumina [up to 1,000,000]"	N
11/25/2008	18840781	Grant	7-Oct-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes	Type 1 diabetes	"563 cases, 1,146 controls, 483 case-parents trios"	"636 families, 3,303 cases, 4,673 controls"	1p22.3	EDG7	rs1983853-?	rs1983853	NR	2E-06		1.2	[1.11-1.29]	"Illumina [up to 1,000,000]"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	10q24.1	TLL2	rs10786284-?	rs10786284	NR	0.000002		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	5q22.2	REEP5	rs469727-?	rs469727	NR	0.000008		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	2p25.3	MYT1L	rs2241685-?	rs2241685	NR	0.000008		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	13q31.3	GPC6	rs7995215-?	rs7995215	NR	1.00E-08		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	15q23	ITGA11	rs7164335-?	rs7164335	NR	1.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	20q11.22	MMP24	rs1555322-?	rs1555322	NR	0.000004		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	2q33.3	CRYGC	rs2242073-?	rs2242073	NR	0.000008		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	12q23.3	NT5DC3	rs4964805-?	rs4964805	NR	0.000005		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	7p15.1	CREB5	rs2237349-?	rs2237349	NR	0.000005		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	16q24.1	ATP2C2	rs10514604-?	rs10514604	NR	8.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	6p21.1	TFEB	rs2842643-?	rs2842643	NR	0.000003		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	17p13.2	ITGAE	rs220470-?	rs220470	NR	1.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	6p21.1	SUPT3H	rs3799977-?	rs3799977	NR	0.000005		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	16q23.3	CDH13	rs11646411-?	rs11646411	NR	0.000007		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	10q25.1	C10orf79	rs515910-?	rs515910	NR	0.000004		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	22q11.22	PPM1F	rs412050-?	rs412050	NR	0.000006		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	9q34.11	DNM1	rs2502731-?	rs2502731	NR	0.000002		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	1p35.1	CSMD2	rs2281597-?	rs2281597	NR	5.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	9q33.1	ASTN2	rs10983238-?	rs10983238	NR	1.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	15q26.1	AK094352	rs7175404-?	rs7175404	NR	6.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	9q34.13	C9orf98	rs11243897-?	rs11243897	NR	6.00E-08		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	2q14.2	MGC33657	rs2587695-?	rs2587695	NR	3.00E-07		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	3p22.1	MOBP	rs864643-?	rs864643	NR	1.00E-08		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	5q13.2	MAP1B	rs2199161-?	rs2199161	NR	0.000002		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	10q22.1	UNC5B	rs16928529-?	rs16928529	NR	0.000004		NR	NR	"Affymetrix [504,219](pooled)"	N
5/7/2009	18839057	Lesch	7-Oct-08	J Neural Transm	http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies	Attention deficit hyperactivity disorder	"343 cases, 304 controls"	NR	15q26.1	MAN2A2	rs2677744-?	rs2677744	NR	0.000001		NR	NR	"Affymetrix [504,219](pooled)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	3q27.2	Intergenic	rs10049246-G	rs10049246	0.59	0.000008	"(int, MW)"	0.6	[NR] unit increase	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	11q21	PIWIL4	rs2212361-C	rs2212361	0.26	9.00E-07	"(int, MW)"	0.97	[NR] unit decrease	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	21q21.1	Intergenic	rs2825388-A	rs2825388	0.4	0.000008	"(int, MC)"	1.06	[NR] unit increase	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	8p23.2	Intergenic	rs4875598-G	rs4875598	0.34	0.000009	"(int, MW)"	0.94	[NR] unit decrease	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	14q24.3	Intergenic	rs2360997-C	rs2360997	0.86	0.000008	"(int, MW)"	1.3	[NR] unit decrease	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	13q12.3	Intergenic	rs1161463-C	rs1161463	0.79	0.000002	"(int, MW)"	1.72	[NR] unit decrease	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan	Attention deficit hyperactivity disorder symptoms (interaction)	909 trios	NR	6p21.2	KIF6	rs4714261-T	rs4714261	0.17	0.000002	"(int, MW)"	0.95	[NR] unit increase	"Perlegen [429,981]"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	17q22	Intergenic	rs8073783-C	rs8073783	0.49	0.000008	"(int, MW)"	1.76	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	18q12.3	Intergenic	rs17664267-T	rs17664267	0.19	0.000007	"(int, MW)"	1.39	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	1q22	RIT1	rs2282301-A	rs2282301	0.23	0.000007	"(int, MW)"	2.88	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	10q22.3	Intergenic	rs2395528-T	rs2395528	0.23	0.000006	"(int, MW)"	1.46	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	3p25.3	SLC6A1	rs9990174-T	rs9990174	0.33	0.000006	"(int, MW)"	2.52	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	8p23.1	MFHAS1	rs332034-A	rs332034	0.85	0.000006	"(int, MW)"	1.05	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	4q23	ADH1C	rs1789891-A	rs1789891	0.14	0.000003	"(int, MW)"	1.47	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	16p13.3	A2BP1	rs6500744-C	rs6500744	0.53	0.000003	"(int, MW)"	0.91	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	5q21.1	Intergenic	rs13188771-A	rs13188771	0.17	0.000002	"(int, MW)"	4.24	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	11q23.2	ZBTB16	rs17116334-T	rs17116334	0.16	0.000009	"(int, MC)"	1.3	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	6p15	Intergenic	rs16880441-G	rs16880441	0.08	0.000009	"(int, MC)"	1.63	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	15q26.2	Intergenic	rs4321143-G	rs4321143	0.28	0.000007	"(int, MC)"	1.13	[NR] unit increase	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	4q22.1	PPM1K	rs893971-T	rs893971	0.6	0.000007	"(int, MC)"	1.15	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	2p21	Intergenic	rs719593-T	rs719593	0.86	0.000005	"(int, MC)"	2.05	[NR] unit decrease	"Perlegen [429,901)"	N
12/9/2008	18846501	Sonuga-Barke	7-Oct-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan	Conduct disorder (interaction)	909 trios	NR	2p22.2	Intergenic	rs604381-A	rs604381	0.32	0.000008	"(int, MW)"	1.26	[NR] unit increase	"Perlegen [429,901)"	N
11/25/2008	18836448	Franke	5-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18836448?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility"	Ulcerative colitis	"1,167 cases, 777 controls"	"1,855 cases, 3,091 controls"	1q32.1	IL10	rs3024505-T	rs3024505	0.15	1.00E-12		1.46	[1.31-1.62]	"Affymetrix [355,262]"	N
11/25/2008	18836448	Franke	5-Oct-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18836448?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility"	Ulcerative colitis	"1,167 cases, 777 controls"	"1,855 cases, 3,091 controls"	6p21.32	"HLA-DRA, BTNL2"	rs9268877-T	rs9268877	0.45	6.00E-18		1.45	[1.33-1.58]	"Affymetrix [355,262]"	N
10/14/2009	19802338	Chasman	1-Oct-08	Circ Cardiovasc Genet	http://www.ncbi.nlm.nih.gov/pubmed/19802338?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	"Genetic loci associated with plasma concentration of LDL-C, HDL-C, triglycerides, ApoA1, and ApoB among 6382 Caucasian women in genome-wide analysis with replication"	Lipid traits	"6,382 Caucasian women"	970 Caucasian individuals	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [314,518]"	N
11/25/2008	18834626	Dehghan	1-Oct-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study	Serum urate	"11,847 individuals"	"14,867 individuals"	4p16.1	SLC2A9	rs16890979-T	rs16890979	0.23	0	(whites)	0.34	[0.30-0.38] SD decrease in serum uric acid level	"Affymetrix and Illumina [up to 530,683]"	N
11/25/2008	18834626	Dehghan	1-Oct-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study	Serum urate	"11,847 individuals"	"14,867 individuals"	6p22.2	SLC17A3	rs1165205-?	rs1165205	0.47	4.00E-29	(whites)	0.09	[0.07-0.11] SD decrease in serum uric acid level	"Affymetrix and Illumina [up to 530,683]"	N
11/25/2008	18834626	Dehghan	1-Oct-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study	Serum urate	"11,847 individuals"	"14,867 individuals"	4q22.1	ABCG2	rs2231142-?	rs2231142	0.11	3.00E-60	(whites)	0.24	[0.20-0.28] SD increase in serum uric acid level	"Affymetrix and Illumina [up to 530,683]"	N
12/9/2008	18991354	Gretarsdottir	1-Oct-08	Ann Neurol	http://www.ncbi.nlm.nih.gov/pubmed/18991354?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke	Ischemic stroke	"1,661 cases, 10,815 controls"	"4,576 cases, 19,343 controls"	4q25	NR	rs2200733-T	rs2200733	0.11	2.00E-10		1.26	[1.17-1.35]	"Illumina [310,881]"	N
11/25/2008	18835860	Mushiroda	1-Oct-08	J Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/18835860?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis	Idiopathic pulmonary fibrosis	"159 Japanese cases, 934 Japanese controls"	"83 Japanese cases, 535 Japanese controls"	5p15.33	TERT	rs2736100-A	rs2736100	0.41	3.00E-08		2.11	[1.61-2.78]	"Illumina [214,508]"	N
11/25/2008	18823527	Abraham	29-Sep-08	BMC Med Genomics	http://www.ncbi.nlm.nih.gov/pubmed/18823527?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study for late-onset Alzheimer's disease using DNA pooling	Alzheimer's disease	"1,082 cases, 1,239 controls"	"1,400 additional controls"	19q13.32	"PVRL2, TOMM40, APOE"	rs6859-A	rs6859	NR	6.00E-14		NR	NR	"Illumina [561,494] (pooled)"	N
11/25/2008	18823527	Abraham	29-Sep-08	BMC Med Genomics	http://www.ncbi.nlm.nih.gov/pubmed/18823527?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A genome-wide association study for late-onset Alzheimer's disease using DNA pooling	Alzheimer's disease	"1,082 cases, 1,239 controls"	"1,400 additional controls"	22q13.33	CPT1B	rs727153-C	rs727153	0.17	0.000003		1.63	[1.37-1.95]	"Illumina [561,494] (pooled)"	N
11/25/2008	18820697	Miyagawa	28-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18820697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variant between CPT1B and CHKB associated with susceptibility to narcolepsy	Narcolepsy	"222 Japanese cases, 389 Japanese controls"	"748 cases, 994 controls"	22q13.33	CPT1B	rs5770917-C	rs5770917	0.17	6.00E-08		1.63	[1.37-1.95]	"Affymetrix [249,133]"	N
11/25/2008	18821564	Mick	26-Sep-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821564?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor	Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder	Attention deficit hyperactivity disorder	187 children	NR	5p15.31	Intergenic	rs11134178-T	rs11134178	0.05	0.000003		NR	NR	"Affymetrix [319,722]"	N
11/25/2008	18821564	Mick	26-Sep-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18821564?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor	Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder	Attention deficit hyperactivity disorder	187 children	NR	22q13.31	Intergenic	rs9627183-C	rs9627183	0.03	0.000003		NR	NR	"Affymetrix [319,722]"	N
12/9/2008	18802019	Burkhardt	18-Sep-08	Arterioscler Thromb Vasc Biol	http://www.ncbi.nlm.nih.gov/pubmed/18802019?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common SNPs in HMGCR in Micronesians and Whites Associated With LDL-Cholesterol Levels Affect Alternative Splicing of Exon13	LDL cholesterol	"2,346 Micronesian individuals"	"1,464 European white cases, 1,467 European white controls"	19q13.32	"APOE, APOC1, APOC4, APOC2"	rs4420638-?	rs4420638	NR	2.00E-07		NR	NR	"Affymetrix [~500,000]"	N
12/9/2008	18802019	Burkhardt	18-Sep-08	Arterioscler Thromb Vasc Biol	http://www.ncbi.nlm.nih.gov/pubmed/18802019?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common SNPs in HMGCR in Micronesians and Whites Associated With LDL-Cholesterol Levels Affect Alternative Splicing of Exon13	LDL cholesterol	"2,346 Micronesian individuals"	"1,464 European white cases, 1,467 European white controls"	5q13.3	HMGCR	rs7703051-A	rs7703051	0.41	1.00E-08		18	[NR] % SD increase	"Affymetrix [~500,000]"	N
11/25/2008	18780872	Liu	17-Sep-08	J Natl Cancer Inst	http://www.ncbi.nlm.nih.gov/pubmed/18780872?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Familial Aggregation of Common Sequence Variants on 15q24-25.1 in Lung Cancer	Lung cancer	"194 cases, 219 controls"	"3,878 cases, 4,831 controls"	15q25.1	"LOC123688, PSMA4, CHRNA3, CHRNA5, CHRNB4"	rs8034191-G	rs8034191	NR	1.00E-08		1.38	[1.17-1.64]	"Affymetrix [up to 722,376]"	N
11/25/2008	18794855	Kiemeney	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794855?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variant on 8q24 confers susceptibility to urinary bladder cancer	Urinary bladder cancer	"1,803 cases, 34,336 controls"	"2,165 cases, 3,800 controls"	8q24.21	"MYC, BC042052"	rs9642880-T	rs9642880	0.45	9.00E-12		1.22	[1.15-1.29]	"Illumina [302,140]"	N
11/25/2008	18794855	Kiemeney	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794855?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Sequence variant on 8q24 confers susceptibility to urinary bladder cancer	Urinary bladder cancer	"1,803 cases, 34,336 controls"	"2,165 cases, 3,800 controls"	3q28	TP63	rs710521-A	rs710521	0.73	1.00E-07		1.19	[1.12-1.27]	"Illumina [302,140]"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	1p13.2	PTPN22	rs6679677-?	rs6679677	0.1	6.00E-42		1.79	[1.65-1.94]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	6p21.32	HLA-DRB1	rs6457620-?	rs6457620	0.5	0		2.55	[2.40-2.71]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	6q23.3	"OLIG3, TNFIP3"	rs6920220-?	rs6920220	0.22	2.00E-09		1.24	[1.16-1.32]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	7q21.2	CDK6	rs42041-G	rs42041	0.24	4E-06		1.11	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	12q13.3	KIF5A-PIP4K2C	rs1678542-C	rs1678542	0.37	9.00E-08		1.12	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	1p36.32	MMEL1-TNFRSF14	rs3890745-T	rs3890745	0.33	1.00E-07		1.12	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	10p15.1	PRKCQ	rs4750316-G	rs4750316	0.2	4E-06		1.14	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	20q13.12	CD40	rs4810485-G	rs4810485	0.25	8.00E-09		1.15	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18794853	Raychaudhuri	14-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants at CD40 and other loci confer risk of rheumatoid arthritis	Rheumatoid arthritis	"3,393 cases, 12,460 controls"	"3,929 cases, 5,807 controls"	9p13.3	CCL21	rs2812378-G	rs2812378	0.34	3.00E-08		1.12	[NR]	"Illumina [818,728] Affymetrix [~340,000] (imputed)"	N
11/25/2008	18760390	Huyghe	12-Sep-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18760390?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait	Hearing impairment	"1,081 individuals"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [169,154]"	N
11/25/2008	18776929	Liu	8-Sep-08	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/18776929?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study	Hip bone size	"501 women, 499 men"	"1,216 women"	2q33.1	PLCL1	rs7595412-A	rs7595412	0.89	2E-06		5	[NR] cm2 increase in hip bone size on women	"Affymetrix [306,823]"	N
11/25/2008	18776911	Hazra	7-Sep-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18776911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Common variants of FUT2 are associated with plasma vitamin B12 levels	Plasma level of vitamin B12	"1,658 women"	"1,059 women"	19q13.3	FUT2	rs492602-G	rs492602	0.49	5.00E-17		0.09	[0.07-0.11] pg/ml decrease	"Illumina [528,134]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	4p16.1	"GLUT9, WDR1"	rs16890979-?	rs16890979	NR	1.00E-11		0.44	[0.32-0.56] mg/dl decrease in uric serum levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	13q33.1	NR	rs4771450-?	rs4771450	NR	2E-06		0.23	[NR] mg/dl decrease in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	2q31.1	NR	rs4668338-?	rs4668338	NR	0.000003		4.29	[NR] mg/dl decrease in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	13q14.11	NR	rs17065323-?	rs17065323	NR	4E-06		4.29	[NR] mg/dl decrease in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	20p12.3	NR	rs6085920-?	rs6085920	NR	0.000006		0.4	[NR] mg/dl decrease in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	3p24.3	NR	rs6442522-?	rs6442522	NR	0.000005		0.05	[NR] mg/dl increase in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18759275	McArdle	1-Sep-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish	Serum uric acid	"408 women, 460 men"	NR	5q31.3	NR	rs3776331-?	rs3776331	NR	8E-06		0.3	[NR] mg/dl increase in uric acid levels	"Affymetrix [361,034]"	N
11/25/2008	18762592	van den Oord	1-Sep-08	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism	Neuroticism	"1,227 individuals"	"1,880 individuals"	14q21.3	MAMDC1	rs12883384-?	rs12883384	NR	7.00E-07		NR	NR	"Affymetrix [420,287]"	N
11/25/2008	18762592	van den Oord	1-Sep-08	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism	Neuroticism	"1,227 individuals"	"1,880 individuals"	7p21.3	NXPH1	rs2349775-?	rs2349775	NR	7E-06		NR	NR	"Affymetrix [420,287]"	N
11/25/2008	18762592	van den Oord	1-Sep-08	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism	Neuroticism	"1,227 individuals"	"1,880 individuals"	8q24.23	AK127771	rs2705293-?	rs2705293	NR	0.000006		NR	NR	"Affymetrix [420,287]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	2q13	"ACOXL,BCL2L11"	rs17483466-G	rs17483466	0.2	2.00E-10		1.39	[1.25-1.53]	"Illumina [345,665]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	19q13.32	"PRKD2,STRN4"	rs11083846-A	rs11083846	0.22	4.00E-09		1.35	[1.22-1.49]	"Illumina [345,665]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	11q24.1	GRAMD1B	rs735665-A	rs735665	0.21	4.00E-12		1.45	[1.31-1.61]	"Illumina [345,665]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	2q37.1	"SP140, SP110"	rs13397985-G	rs13397985	0.19	6.00E-10		1.41	[1.26-1.57]	"Illumina [345,665]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	15q23	Intergenic	rs7176508-A	rs7176508	0.37	5.00E-12		1.37	[1.26-1.50]	"Illumina [345,665]"	N
11/25/2008	18758461	Di Bernardo	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia	Chronic lymphocytic leukemia	"505 cases, 1,438 controls"	"1,024 cases, 1,677 controls"	6p25.3	IRF4	rs872071-G	rs872071	0.54	2.00E-20		1.54	[1.41- 1.69]	"Illumina [345,665]"	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	20q13.33	TNFRSF6B	rs2315008-G	rs2315008	0.69	9.00E-15		1.36	[1.05-1.76]	Illumina [NR]	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	21q22.2	PSMG1	rs2836878-?	rs2836878	0.72	4.00E-12		1.41	[1.08-1.84]	Illumina [NR]	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	1p31.3	IL23R	rs11209026-?	rs11209026	0.94	7.00E-11		2.56	[1.92-3.45]	Illumina [NR]	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	16q12.1	NOD2	rs5743289-T	rs5743289	0.17	4.00E-10		1.46	[1.29-1.64]	Illumina [NR]	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	9q32	TNFSF15	rs6478109-?	rs6478109	0.69	3.00E-08		1.36	[1.22-1.52]	Illumina [NR]	N
11/25/2008	18758464	Kugathasan	31-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease	Inflammatory bowel disease	"1,011 cases, 4,250 controls"	"1,922 cases, 14,124 controls"	6p21.32	HLA-DQA1	rs477515-?	rs477515	0.69	1.00E-08		1.38	[1.23-1.54]	Illumina [NR]	N
11/25/2008	18729187	Galvan	26-Aug-08	Int J Cancer	http://www.ncbi.nlm.nih.gov/pubmed/18729187?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A polygenic model with common variants may predict lung adenocarcinoma risk in humans	Lung adenocarcinoma	"482 cases, 522 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [~318,000] (pooled)"	N
11/25/2008	18846228	Weidinger	22-Aug-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846228?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus	Serum IgE levels	"1,530 individuals"	"9,769 individuals"	5q31.1	RAD50	rs2040704-?	rs2040704	0.23	4.00E-08		13.9	[NR] % increase	"Affymetrix [353,569]"	N
11/25/2008	18846228	Weidinger	22-Aug-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18846228?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus	Serum IgE levels	"1,530 individuals"	"9,769 individuals"	1q23.2	FCER1A	rs2251746-C	rs2251746	0.26	2.00E-20		19.2	[NR] % decrease	"Affymetrix [353,569]"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	11q14.1	NR	rs12290811-A	rs12290811	0.15	4E-06		1.2	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	2q11.2	Intergenic	rs2314398-?	rs2314398	0.69	0.000003		1.17	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	15q14	"C15orf53, RASGRP1"	rs12899449-?	rs12899449	0.72	4.00E-07		1.2	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	10q21.2	ANK3	rs10994336-T	rs10994336	0.05	9.00E-09		1.45	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	12q13.12	CACNA1C	rs1006737-A	rs1006737	0.32	7.00E-08		1.18	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	10q22.3	NR	rs703965-?	rs703965	0.54	8E-06		1.15	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	3p26.2	NR	rs1601875-?	rs1601875	0.5	7E-06		1.14	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	18p11.32	NR	rs7226677-G	rs7226677	0.12	7E-06		1.24	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	15q25.1	NR	rs2278702-?	rs2278702	0.83	0.000006		1.21	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	11q24.2	NR	rs544368-T	rs544368	0.12	0.000006		1.22	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	9q31.3	NR	rs7042161-?	rs7042161	0.65	0.000006		1.15	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	1p21.2	NR	rs1948368-?	rs1948368	0.51	0.000006		1.15	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	3p24.3	NR	rs11720452-?	rs11720452	0.58	0.000005		1.15	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	14q11.2	NR	rs12436436-C	rs12436436	0.08	0.000005		1.3	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	14q13.1	NR	rs8015959-T	rs8015959	0.02	0.000005		1.59	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	3p24.3	NR	rs3821396-A	rs3821396	0.11	0.000005		1.23	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	9q33.3	NR	rs4130590-?	rs4130590	0.56	0.000003		1.16	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	6q25.2	NR	rs17082664-G	rs17082664	0.13	4E-06		1.22	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	15q14	NR	rs16966460-G	rs16966460	0.1	4E-06		1.26	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	3p22.3	NR	rs4380451-?	rs4380451	0.73	4E-06		1.18	[NR]	"Affymetrix [1,769,948] imputed"	N
11/25/2008	18711365	Ferreira	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder	Bipolar disorder	"4,387 cases, 6,209 controls"	NR	9p13.3	NR	rs216345-T	rs216345	0.37	4E-06		1.15	[NR]	"Affymetrix [1,769,948] imputed"	N
4/10/2009	18711366	Unoki	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations	Type 2 diabetes	"194 Japanese cases, 1,558 Japanese controls"	"4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)"	6p22.3	CDKAL1	rs4712524-G	rs4712524	0.42	3.00E-10		1.22	[1.15-1.31]	"Affymetrix [207,097]"	N
4/10/2009	18711366	Unoki	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations	Type 2 diabetes	"194 Japanese cases, 1,558 Japanese controls"	"4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)"	3q27.2	IGF2BP2	rs6769511-C	rs6769511	0.32	1.00E-09		1.23	[1.15-1.31]	"Affymetrix [207,097]"	N
4/10/2009	18711366	Unoki	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations	Type 2 diabetes	"194 Japanese cases, 1,558 Japanese controls"	"4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)"	11p15.4	KCNQ1	rs2237897-C	rs2237897	0.61	1.00E-16		1.33	[1.24-1.41]	"Affymetrix [207,097]"	N
4/3/2009	18711367	Yasuda	17-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18711367?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus	Type 2 diabetes	"187 Japanese cases, 1,504 Japanese controls"	"6,552 Asian cases, 6,621 Asian controls, 2,830 cases, 3,740 controls (Swedish)"	11p15.5	KCNQ1	rs2237892-C	rs2237892	0.61	2.00E-42		1.4	[1.34-1.47]	"Invader [82,343]"	N
11/25/2008	18685109	Shlien	12-Aug-08	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/18685109?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome	TP53 carriage	"53 carriers, 70 controls"	770 individuals	Pending	Pending	Pending		Pending	Pending	Pending	Pending	Pending	"Affymetrix [3,884 CNVs]"	Y
11/25/2008	18690218	Hofmann	10-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18690218?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis	Sarcoidosis	"499 cases, 490 controls"	"1,649 cases, 1,832 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [375,771]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	2q32.3	STAT4	rs3821236-?	rs3821236	0.19	8.00E-11		1.49	[NR]	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	4q28.3	Intergenic	rs2313132-?	rs2313132	0.12	8E-06		NR	NR	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	17p12	Intergenic	rs12949531-?	rs12949531	0.22	8E-06		NR	NR	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	8p23.1	BLK	rs2618476-?	rs2618476	0.26	2.00E-08		1.29	[NR]	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	16p11.2	ITGAM	rs11150610-?	rs11150610	0.42	2E-06		NR	NR	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	6q23.3	TNFAIP3	rs5029939-?	rs5029939	0.03	3.00E-12		2.28	[NR]	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	10q11.22	c10orf64	rs11101442-?	rs11101442	0.32	0.000003		NR	NR	"Affymetrix [313,238]"	N
11/25/2008	18677312	Graham	1-Aug-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"431 cases, 2,155 controls"	740 trios	2p16.3	Intergenic	rs17039212-?	rs17039212	0.1	0.000009		NR	NR	"Affymetrix [313,238]"	N
11/25/2008	18668548	Julia	1-Aug-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18668548?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility	Rheumatoid arthritis	"400 cases, 400 controls"	"410 cases, 394 controls"	18q23	SALL3	rs2002842-A	rs2002842	0.49	0.000006		1.61	[NR]	"Illumina [299,918]"	N
11/25/2008	18668548	Julia	1-Aug-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18668548?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility	Rheumatoid arthritis	"400 cases, 400 controls"	"410 cases, 394 controls"	6p21.32	"HLA-DQA1, HLA-DQA2"	rs6457617-?	rs6457617	NR	1.00E-09		NR	NR	"Illumina [299,918]"	N
11/25/2008	18677311	O'Donovan	30-Jul-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of loci associated with schizophrenia by genome-wide association and follow-up	Schizophrenia	"479 cases, 2,937 controls"	"6,666 cases, 9,897 controls"	16p13.12	Intergenic	rs7192086-T	rs7192086	0.24	0.000006		1.12	[NR]	"Affymetrix [362,532]"	N
11/25/2008	18677311	O'Donovan	30-Jul-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of loci associated with schizophrenia by genome-wide association and follow-up	Schizophrenia	"479 cases, 2,937 controls"	"6,666 cases, 9,897 controls"	11p14.1	Intergenic	rs1602565-C	rs1602565	0.11	0.000003		1.16	[NR]	"Affymetrix [362,532]"	N
11/25/2008	18677311	O'Donovan	30-Jul-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of loci associated with schizophrenia by genome-wide association and follow-up	Schizophrenia	"479 cases, 2,937 controls"	"6,666 cases, 9,897 controls"	2q32.1	ZNF804A	rs1344706-T	rs1344706	0.59	2.00E-07		1.12	[NR]	"Affymetrix [362,532]"	N
11/25/2008	18660810	Schormair	27-Jul-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18660810?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome	Restless legs syndrome	"628 cases, 1,644 controls"	"1,835 cases, 3,111 controls"	9p24.1	PTPRD	rs1975197-T	rs1975197	0.16	6.00E-09		1.31	[1.20-1.44]	"Affymetrix [208,733]"	N
11/25/2008	18660810	Schormair	27-Jul-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18660810?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome	Restless legs syndrome	"628 cases, 1,644 controls"	"1,835 cases, 3,111 controls"	9p23	PTPRD	rs4626664-A	rs4626664	0.12	6.00E-10		1.44	[1.31-1.59]	"Affymetrix [208,733]"	N
11/25/2008	18650507	The SEARCH Collaborative Group	23-Jul-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18650507?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	SLCO1B1 Variants and Statin-Induced Myopathy--A Genomewide Study	Response to statin therapy	"85 cases, 90 controls"	"19,856 individuals"	12p12.1	SLCO1B1	rs4149056-C	rs4149056	0.13	2.00E-09		4.5	[2.60-7.70]	"Illumina [316,184]"	N
11/25/2008	18723019	Franke	21-Jul-08	Gastroenterology	http://www.ncbi.nlm.nih.gov/pubmed/18723019?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study anaylsis in sarcoidosis and Crohn disease unravels a common susceptibility locus on 10p12.2	Crohn's disease and Sarcoidosis (combined)	"382 CD cases, 398 SA cases, 394 controls"	"660 CD cases, 657 SA cases, 1,091 controls"	10p12.2	C10orf67	rs1398024-A	rs1398024	0.25	0.000004		1.23	[1.04-1.45]	"Affymetrix [83,360]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	9p21.2	IFNK	rs7046653-A	rs7046653	0.26	5.00E-07		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	20q12	MAFB	rs6028945-T	rs6028945	0.12	2.00E-07		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	7q21.3	PON1	rs854555-A	rs854555	0.34	2E-06		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	4p15.1	CENTD1	rs437943-G	rs437943	0.33	4E-06		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	1p22.3	LMO4	rs983332-A	rs983332	0.21	0.000005		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	6q26	QKI	rs10945919-G	rs10945919	0.32	3.00E-07		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	20p11.21	CST5	rs6138150-T	rs6138150	0.84	0.000003		NR	NR	"Illumina [283,348]"	N
11/25/2008	18615156	Liu	10-Jul-08	Mol Med	http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis	Treatment response to TNF antagonists	89 cases	NR	2q24.3	LASS6	rs13393173-A	rs13393173	0.12	4E-06		NR	NR	"Illumina [283,348]"	N
11/25/2008	18604267	Pare	4-Jul-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women"	Soluble ICAM-1	"4,570 women"	"2,008 women"	9q34.2	ABO	rs507666-G	rs507666	0.2	5.00E-29		17.73	[NR] umol/L decrease	"Illumina [336,108]"	N
11/25/2008	18604267	Pare	4-Jul-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women"	Soluble ICAM-1	"4,570 women"	"2,008 women"	19p13.2	ICAM1	rs1799969-G	rs1799969	0.12	4.00E-47		28.19	[NR] umol/L decrease	"Illumina [336,108]"	N
11/25/2008	18604267	Pare	4-Jul-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women"	Soluble ICAM-1	"4,570 women"	"2,008 women"	19p13.2	ICAM1	rs5498-A	rs5498	0.43	5.00E-25		13.22	[NR] umol/L increase	"Illumina [336,108]"	N
11/25/2008	18604267	Pare	4-Jul-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women"	Soluble ICAM-1	"4,570 women"	"2,008 women"	19p13.2	ICAM1	rs281437-?	rs281437	0.3	3.00E-10		10.1	[NR] umol/L increase	"Illumina [336,108]"	N
11/25/2008	18601904	Bae	2-Jul-08	Biochem Biophys Res Commun	http://www.ncbi.nlm.nih.gov/pubmed/18601904?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population	Subarachnoid aneurysmal hemorrhage	"203 cases, 294 controls"	NR	Pending	Pending	Pending		Pending	Pending	Pending	Pending	Pending	"Illumina [317,503]"	Y
11/25/2008	18594024	Sarasquete	1-Jul-08	Blood	http://www.ncbi.nlm.nih.gov/pubmed/18594024?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis	Osteonecrosis of the jaw	"21 cases, 64 controls"	NR	10q23.33	CYP2C8	rs1934951-T	rs1934951	0.12	1.00E-06		12.75	[3.7-43.5]	"Affymetrix [339,972]"	N
11/25/2008	18591461	Turner	30-Jun-08	Hypertension	http://www.ncbi.nlm.nih.gov/pubmed/18591461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic	Response to diuretic therapy	"194 blacks, 195 whites"	NR	12q15	"LYZ, YEATS4, FRS2"	3-SNP haplotype	"rs317689,rs315135,rs7297610"	NR	0.000006		NR	NR	"Affymetrix [up to 102,334]"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	2q37.1	ATG16L1	rs3828309-G	rs3828309	0.53	2.00E-32		1.25	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	16q12.1	NOD2	rs2066847-C	rs2066847	0.02	3.00E-24		3.99	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	10q24.2	NKX2-3	rs11190140-T	rs11190140	0.48	3.00E-16		1.2	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	9q32	TNFSF15	rs4263839-G	rs4263839	0.68	3.00E-10		1.22	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	5q33.1	IRGM	rs11747270-G	rs11747270	0.09	3.00E-16		1.33	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	5q31.1	Intergenic	rs2188962-T	rs2188962	0.43	2.00E-18		1.25	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	5p13.1	PTGER4	rs4613763-C	rs4613763	0.13	7.00E-27		1.32	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	10q21.2	ZNF365	rs10995271-C	rs10995271	0.39	4.00E-20		1.25	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	13q14.11	Unknown	rs3764147-G	rs3764147	0.22	2.00E-13		1.25	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	5q33.3	IL12B	rs10045431-C	rs10045431	0.71	4.00E-13		1.11	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	6q27	CCR6	rs2301436-T	rs2301436	0.46	1.00E-12		1.21	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	17q21.2	STAT3	rs744166-A	rs744166	0.57	7.00E-12		1.18	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	6q21	Unknown	rs7746082-C	rs7746082	0.29	2.00E-10		1.17	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	3p21.31	MST1	rs3197999-A	rs3197999	0.27	1.00E-12		1.2	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	18p11.21	PTPN2	rs2542151-G	rs2542151	0.15	5.00E-17		1.35	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	1p31.3	IL23R	rs11465804-T	rs11465804	0.93	7.00E-63		2.5	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	1p13.2	PTPN22	rs2476601-G	rs2476601	0.9	1.00E-08		1.31	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	1q23.2	ITLN1	rs2274910-C	rs2274910	0.68	1.00E-09		1.14	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	1q24.3	Intergenic	rs9286879-G	rs9286879	0.24	2.00E-09		1.19	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	1q32.1	Intergenic	rs11584383-T	rs11584383	0.7	1.00E-11		1.18	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	6p22.3	CDKAL1	rs6908425-C	rs6908425	0.78	9.00E-10		1.21	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	7p12.2	Intergenic	rs1456893-A	rs1456893	0.68	5.00E-09		1.2	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	8q24.13	Intergenic	rs1551398-A	rs1551398	0.62	5.00E-09		1.08	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	9p24.1	JAK2	rs10758669-C	rs10758669	0.35	3.00E-09		1.12	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	10p11.21	Intergenic	rs17582416-G	rs17582416	0.35	2.00E-09		1.16	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	11q13.5	C11orf30	rs7927894-T	rs7927894	0.39	1.00E-09		1.16	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	12q12	"LRRK2, MUC19"	rs11175593-T	rs11175593	0.02	3.00E-10		1.54	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	17q12	ORMDL3	rs2872507-A	rs2872507	0.47	5.00E-09		1.12	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	21q21.1	Intergenic	rs1736135-T	rs1736135	0.57	7.00E-09		1.18	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18587394	Barrett	29-Jun-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease	Crohn's disease	"3,230 cases 4,829 controls"	"1,339 trios, 2,325 cases, 1,809 controls"	21q22.3	ICOSLG	rs762421-G	rs762421	0.39	1.00E-09		1.13	[NR]	"Affymetrix and Illumina [635,547] (imputed)"	N
11/25/2008	18576341	Behrens	24-Jun-08	Arthritis Rheum	http://www.ncbi.nlm.nih.gov/pubmed/18576341?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis	Arthritis (juvenile idiopathic)	"130 cases 1,952 controls"	NR	6p21.32	HLA-DRB1	rs2395148-?	rs2395148	NR	2.00E-10		5.37	[3.02-9.56]	"Illumina [524,684]"	N
11/25/2008	18451265	Bouatia-Naji	19-Jun-08	Science	http://www.ncbi.nlm.nih.gov/pubmed/18451265?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Polymorphism Within the G6PC2 Gene is Associated with Fasting Plasma Glucose Levels	Fasting plasma glucose	654 normoglycemic individuals	"9,353 individuals"	2q24.3	G6PC2	rs560887-A	rs560887	0.3	4.00E-23		0.06	[0.05-0.08] mmol/l decrease	"Illumina [392,935]"	N
11/25/2008	18535201	Cooper	5-Jun-08	Blood	http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose	Warfarin maintenance dose	181 individuals	374 individuals	12p13.33	CACNA1C	rs216013-?	rs216013	NR	9.00E-07		NR	NR	"Illumina [538,629]"	N
11/25/2008	18535201	Cooper	5-Jun-08	Blood	http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose	Warfarin maintenance dose	181 individuals	374 individuals	10q23.33	CYP2C9	rs4086116-?	rs4086116	NR	6.00E-12		NR	NR	"Illumina [538,629]"	N
11/25/2008	18535201	Cooper	5-Jun-08	Blood	http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose	Warfarin maintenance dose	181 individuals	374 individuals	16p11.2	VKORC1	rs10871454-?	rs10871454	NR	5.00E-34		NR	NR	"Illumina [538,629]"	N
11/25/2008	18521185	Chen	4-Jun-08	J Clin Invest	http://www.ncbi.nlm.nih.gov/pubmed/18521185?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels	Fasting plasma glucose	"5,088 nondiabetic individuals"	"18,436 nondiabetic individuals"	2q24.3	"G6PC2,ABCB11"	rs563694-C	rs563694	0.34	4.00E-07		NR	NR	"Illumina [315,635]"	N
11/25/2008	18519826	Uhl	4-Jun-08	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18519826?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Molecular genetics of successful smoking cessation: convergent genome-wide association study results	Smoking cessation	"241 cases, 309 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~500,000] (pooled)"	N
11/25/2008	18521090	Lavedan	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521090?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of the NPAS3gene and five other loci with response of the antipsychotic iloperidone identified in a whole genome association study	Response to iloperidone treatment (PANSS-T score)	106 individuals	104 individuals	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [334,563]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	2q31.3	CERKL	rs993648-T	rs993648	NR	0.000003		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	10q23.1	NRG3	rs4933824-T	rs4933824	NR	2E-06		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	15q26.1	SLCO3A1	rs3924426-T	rs3924426	NR	2E-06		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	4q32.3	PALLD	rs17054392-C	rs17054392	NR	0.000003		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	18q12.2	BRUNOL4	rs4799915-T	rs4799915	NR	0.000003		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18521091	Volpi	3-Jun-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia	Response to iloperidone treatment (QT prolongation)	183 individuals	NR	14q12	NUBPL	rs7142881-A	rs7142881	NR	2E-06		NR	NR	"Affymetrix [339,272]"	N
11/25/2008	18488026	Brown	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488026?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common sequence variants on 20q11.22 confer melanoma susceptibility	Melanoma	"864 cases, 864 controls"	"1,230 cases, 1,251 controls"	20q11.22	CDC91L1	rs910873-T	rs910873	0.09	1.00E-15		1.75	[1.53-2.01]	"Illumina [535,150] (pooled)"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Blond vs. brown hair color	"5,130 individuals"	"3,330 individuals"	11q13.2	TPCN2	rs35264875-T	rs35264875	0.22	4.00E-30		2.49	[1.96-3.15]	"Illumina [316,515]"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Blue vs. green eyes	"5,130 individuals"	"3,330 individuals"	9p23	TYRP1	rs1408799-C	rs1408799	0.75	6.00E-17		1.4	[1.25-1.57]	"Illumina [316,515]"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Burning and freckling	"5,130 individuals"	"3,330 individuals"	20q11.22	ASIP	rs1015362-G + rs4911414-T	"rs1015362,rs4911414"	0.08	6.00E-37		2.56	[2.06-3.18]	"Illumina [316,515]"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Freckles	"5,130 individuals"	"3,330 individuals"	20q11.22	ASIP	rs1015362-G + rs4911414-T	"rs1015362,rs4911414"	0.08	8.00E-29		1.95	[1.65-2.32]	"Illumina [316,515]"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Red vs. non-red hair color	"5,130 individuals"	"3,330 individuals"	20q11.22	ASIP	rs1015362-G + rs4911414-T	"rs1015362,rs4911414"	0.08	3.00E-09		1.76	[1.34-2.31]	"Illumina [316,515]"	N
11/25/2008	18488028	Sulem	18-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two newly identified genetic determinants of pigmentation in Europeans	Skin sensitivity to sun	"5,130 individuals"	"3,330 individuals"	20q11.22	ASIP	rs1015362-G + rs4911414-T	"rs1015362,rs4911414"	0.08	2.00E-24		1.76	[1.49-2.08]	"Illumina [316,515]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	5p13.3	MATP	rs28777-C	rs28777	NR	1.00E-17		0.46	[0.36-0.56] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	Intergenic	rs8033165-T	rs8033165	NR	5.00E-11		0.12	[0.08-0.16] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	14q32.12	SLC24A4	rs12896399-G	rs12896399	NR	8.00E-21		0.18	[0.14-0.22] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	HERC2	rs12913832-A	rs12913832	NR	4.00E-103		0.44	[0.40-0.48] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	6p25.3	IRF4	rs12203592-T	rs12203592	NR	7.00E-127		0.35	[0.33-0.37] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	OCA2	rs11855019-G	rs11855019	NR	2.00E-24		0.28	[0.22-0.34] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. blond hair color	"2,287 women"	"up to 8,465 individuals"	6p25.3	EXOC2	rs6918152-A	rs6918152	NR	6.00E-08		0.11	[0.07-0.15] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	HERC2	rs12913832-A	rs12913832	NR	1.00E-77		0.44	[0.40-0.48] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	6p25.3	EXOC2	rs6918152-A	rs6918152	NR	5.00E-07		0.11	[0.07-0.15] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	5p13.3	MATP	rs28777-C	rs28777	NR	9.00E-14		0.46	[0.34-0.58] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	16q24.3	MC1R	rs258322-T	rs258322	NR	2.00E-23		0.36	[0.28-0.44] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	6p25.3	IRF4	rs12203592-T	rs12203592	NR	9.00E-28		0.31	[0.25-0.36] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	Intergenic	rs8033165-T	rs8033165	NR	2.00E-12		0.15	[0.11-0.19] increase in hair color score	"Illumina [528,173]"	N
11/25/2008	18483556	Han	16-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation	Black vs. red hair color	"2,287 women"	"up to 8,465 individuals"	15q13.1	OCA2	rs11855019-G	rs11855019	NR	6.00E-20		0.29	[0.23-0.35] decrease in hair color score	"Illumina [528,173]"	N
11/25/2008	18463370	Maris	9-May-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18463370?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma	Neuroblastoma	"1,032 cases, 2,043 controls"	"720 cases, 2,128 controls"	6p22.3	"FLJ22536, FLJ44180"	rs6939340-G	rs6939340	0.5	9.00E-15		1.37	[1.27-1.49]	"Illumina [464,934]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	12q12	"PDZRN4,CNTN1"	rs1880887-?	rs1880887	0.03	1.00E-10	(Alkaline phosphatase)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	12q24.11	ATP2A2	rs11065611-?	rs11065611	0.06	1.00E-07	(Alpha-1 globulin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	12q24.33	GPR133	rs10466868-?	rs10466868	0.12	1.00E-06	(Erythropoeitin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	13q12.11	FGF3	rs17369571-?	rs17369571	0.16	1.00E-07	(IL1RA)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	13q12.2	SACS	rs4770433-?	rs4770433	0.4	4E-06	(IL12)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	15q15.2	CDAN1	rs16957063-?	rs16957063	0.01	5.00E-07	(Ft4)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	15q21.1	DUT	rs11637235-?	rs11637235	0.28	0.000003	(Adiponectin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	16q23.2	BCM01	rs4889294-?	rs4889294	0.47	5.00E-07	(IL1B)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	17p12	HS3ST3B1	rs3848445-?	rs3848445	0.05	8.00E-09	(Ft3)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	17q25.3	C17orf62	rs9303029-?	rs9303029	0.08	4.00E-07	(Free IGF1)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	18q11.2	OSBPL1A	rs9635963-?	rs9635963	0.18	2.00E-07	(SHBG)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	18q12.1	DSC3	rs2729409-?	rs2729409	0.26	0.000003	(Parathyroid hormone)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	19p13.2	ANGPTL6	rs8109578-?	rs8109578	0.08	4.00E-07	(TSH)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	11q23.1	IL18	rs2250417-A	rs2250417	0.44	7.00E-13	(IL18)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	1q21.3	IL6R	rs4129267-C	rs4129267	0.37	2.00E-57	(sIL-6R)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	17q12	CCL4L2	rs4796217-T	rs4796217	0.34	4.00E-21	(MIPb)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6q26	LPA	rs7770628-T	rs7770628	0.49	4.00E-10	(LPA)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	22q11.23	GGT1	rs5751901-T	rs5751901	0.39	2.00E-07	(GGT1)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	9q34.2	ABO	rs505922-?	rs505922	0.34	7.00E-40	(TNFA)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	17p13.1	SHBG	rs6761-?	rs6761	0.31	3.00E-07	(SHBG)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	1q23.2	CRP	rs12093699-?	rs12093699	0.29	0.000006	(CRP)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2q13	IL1RN	rs6761276-?	rs6761276	0.37	7E-06	(IL1RA)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	1p21.1	COL11A	rs10874639-?	rs10874639	0.12	0.000003	(Fibrinogen)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	1q21.1	CHD1L	rs4950322-?	rs4950322	0.21	2.00E-07	(Resistin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	1q21.1	CHD1L	rs4950322-?	rs4950322	0.21	7.00E-07	(Hgb)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2p15	LOC51057	rs11683229-?	rs11683229	0.15	0.000006	(IL6)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2p13.3	DYSF	rs2900976-?	rs2900976	0.3	1.00E-06	(Albumin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2p12	CTNNA2	rs11695685-?	rs11695685	0.3	5.00E-07	(IL10)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2p11.2	SH2D6	rs7577642-?	rs7577642	0.27	7E-06	(sIL-6R)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	2q23.1	EPC2	rs10191411-?	rs10191411	0.32	4E-06	(IL8)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	3p12.3	ROBO1	rs9834373-?	rs9834373	0.17	4E-06	(GP130)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	5q35.1	DOCK2	rs169082-?	rs169082	0.48	1.00E-06	(Leptin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6p21.33	HLA-C	rs9461688-?	rs9461688	0.31	4E-06	(IL18)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6q11.1	KHDRBS2	rs6455128-?	rs6455128	0.19	3.00E-07	(GOT (AST))	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6q22.31	GJA1	rs4541776-?	rs4541776	0.33	2E-06	(GGT)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6q23.2	EYA4	rs9402515-?	rs9402515	0.09	1.00E-06	(Alpha-2 macroglobulin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	6q24.3	SASH1	rs6930337-?	rs6930337	0.06	1.00E-06	(insulin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	7p21.3	NXPH1	rs1285407-?	rs1285407	0.35	1.00E-06	(TGF-b1)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	8q21.11	"GDAP1,PI15"	rs6472866-?	rs6472866	0.42	8.00E-07	(myoglobin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	8q24.21	FAM49B	rs10092658-?	rs10092658	0.07	0.000006	(Aldolase)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	9q22.2	"GADD45G,DIRAS2"	rs2081670-?	rs2081670	0.15	0.000003	(MIP-1b)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	9q31.2	TMEM38B	rs4742971-?	rs4742971	0.11	8.00E-07	(GPT (ALT))	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	10p12.33	CACNB2	rs7076247-?	rs7076247	0.37	0.000006	(CRP)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	10p11.21	"FZD8,ANKRD30A"	rs1779876-?	rs1779876	0.1	0.000003	(Lipoprotein A)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	11p15.5	KCNQ1	rs2237878-?	rs2237878	0.07	0.000001	(Lactic dehydrogenase)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	11q14.1	DLG2	rs3885683-?	rs3885683	0.11	8E-06	(MCP1)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	11q23.3	PAFAH1B2	rs7112513-?	rs7112513	0.13	6.00E-09	(Soluble transferrin receptor)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	11q24.2	KIRREL3	rs1939992-?	rs1939992	0.26	1.00E-06	(Total IGF-1)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18464913	Melzer	9-May-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)	Protein quantitative trait loci	"1,200 individuals"	NR	12p12.3	EPS8	rs17415853-?	rs17415853	0.02	7.00E-07	(Ferritin)	NR	NR	"Illumina [496,032]"	N
11/25/2008	18463975	Kibriya	8-May-08	Breast Cancer Res Treat	http://www.ncbi.nlm.nih.gov/pubmed/18463975?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	A pilot genome-wide association study of early-onset breast cancer	Breast cancer	"30 cases, 30 controls"	NR	2q37.1	GLG1	3-SNP haplotype 1	rs10871290	0.34	4.00E-07		NR	NR	"Affymetrix [200,220]"	N
11/25/2008	18471798	Valdes	8-May-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18471798?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide Association Scan Identifies a Prostaglandin-Endoperoxide Synthase 2 Variant Involved in Risk of Knee Osteoarthritis	Knee osteoarthritis	"357 cases, 285 controls"	"1,177 cases, 2,372 controls"	2q33.3	PARD3B	rs1207421-?	rs1207421	0.09	0.000006		1.46	[1.24-1.73]	"Illumina [413,461]"	N
11/25/2008	18471798	Valdes	8-May-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18471798?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide Association Scan Identifies a Prostaglandin-Endoperoxide Synthase 2 Variant Involved in Risk of Knee Osteoarthritis	Knee osteoarthritis	"357 cases, 285 controls"	"1,177 cases, 2,372 controls"	1q31.1	"PTGS2, PLA2G4A"	rs4140564-?	rs4140564	0.05	0.000003		1.59	[1.31-1.94]	"Illumina [413,461]"	N
11/25/2008	18454146	Chambers	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common genetic variation near MC4R is associated with waist circumference and insulin resistance	Waist circumference and related phenotypes	"2,684 Asian Indian men"	"11,955 Asian Indian and European individuals"	2p23.3	GCKR	rs1260326-?	rs1260326	NR	4.00E-08	(triglycerides)	NR	NR	"Illumina [308,067]"	N
11/25/2008	18454146	Chambers	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common genetic variation near MC4R is associated with waist circumference and insulin resistance	Waist circumference and related phenotypes	"2,684 Asian Indian men"	"11,955 Asian Indian and European individuals"	18q21.32	MC4R	rs12970134-A	rs12970134	0.36	2.00E-09	(waist circumference)	0.88	[0.59-1.17] cm increase	"Illumina [308,067]"	N
11/25/2008	18454146	Chambers	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common genetic variation near MC4R is associated with waist circumference and insulin resistance	Waist circumference and related phenotypes	"2,684 Asian Indian men"	"11,955 Asian Indian and European individuals"	16q13	CETP	rs3764261-?	rs3764261	NR	1.00E-27	(HDL cholesterol)	NR	NR	"Illumina [308,067]"	N
11/25/2008	18454146	Chambers	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common genetic variation near MC4R is associated with waist circumference and insulin resistance	Waist circumference and related phenotypes	"2,684 Asian Indian men"	"11,955 Asian Indian and European individuals"	8p21.3	LPL	rs2083637-?	rs2083637	NR	0.000005	(HDL cholesterol)	NR	NR	"Illumina [308,067]"	N
11/25/2008	18454148	Loos	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454148?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Common variants near MC4R are associated with fat mass, weight and risk of obesity"	Body mass index	"16,876 individuals"	"60,352 individuals"	16q12.2	FTO	rs1121980-?	rs1121980	NR	4.00E-08		0.06	[0.04-0.08] unit increase in log(BMI)	"Affymetrix [344,883]"	N
11/25/2008	18454148	Loos	4-May-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18454148?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Common variants near MC4R are associated with fat mass, weight and risk of obesity"	Body mass index	"16,876 individuals"	"60,352 individuals"	18q21.32	MC4R	rs17782313-C	rs17782313	0.24	3.00E-15		0.05	[0.04-0.06] unit increase in log(BMI)	"Affymetrix [344,883]"	N
11/25/2008	18449908	Poduslo	30-Apr-08	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/18449908?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome Screen of Late-Onset Alzheimer's Extended Pedigrees Identifies TRPC4AP by Haplotype Analysis	Alzheimer's disease	"29 siblings from 2 affected families, 60 unrelated controls"	"199 patients, 85 spouses"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [469,218]"	N
11/25/2008	18455228	Richards	29-Apr-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18455228?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study"	Bone mineral density	"2,094 women"	"6,463 individuals"	8q24.12	TNFRSF11B	rs4355801-A	rs4355801	0.53	8.00E-10		0.09	[NR] SD decrease	"Illumina [314,075]"	N
11/25/2008	18455228	Richards	29-Apr-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18455228?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study"	Bone mineral density	"2,094 women"	"6,463 individuals"	11q13.2	LRP5	rs3736228-T	rs3736228	0.14	6.00E-12		0.13	[NR] SD decrease	"Illumina [314,075]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	18q21.33	RANK	rs3018362-A	rs3018362	0.35	1.00E-06		0.07	[0.04-0.10] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	13q14.11	RANKL	rs9594738-T	rs9594738	0.56	2.00E-08		0.1	[0.06-0.13] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	1p36.12	ZBTB40	rs7524102-A	rs7524102	0.82	5.00E-16		0.15	[0.11-0.19] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	6q25.1	ESR1	rs1038304-G	rs1038304	0.47	5.00E-09		0.08	[0.06-0.11] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	8q24.12	OPG	rs6993813-C	rs6993813	0.5	3.00E-11		0.09	[0.07-0.12] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (hip)	"5,861 individuals"	"7,925 individuals"	6q25.1	"ESR1, C6orf97"	rs4870044-T	rs4870044	0.28	2.00E-07		0.08	[0.05-0.11] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	13q14.11	RANKL	rs9594759-T	rs9594759	0.62	2.00E-21		0.17	[0.14-0.21] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	8q24.12	OPG	rs6469804-A	rs6469804	0.51	7.00E-15		0.12	[0.09-0.15] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	6p25.1	ESR1	rs4870044-T	rs4870044	0.28	2.00E-11		0.11	[0.08-0.14] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	6p21.32	"MHC, C6orf10"	rs3130340-T	rs3130340	0.79	1.00E-07		0.1	[0.06-0.13] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	1p36.12	ZBTB40	rs7524102-A	rs7524102	0.82	9.00E-09		0.11	[0.07-0.15] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	6q25.1	"ESR1, C6orf97"	rs1038304-G	rs1038304	0.47	4.00E-11		0.1	[0.07-0.13] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	2p16.2	SPTBN1	rs11898505-G	rs11898505	0.67	8.00E-07		0.08	[0.05-0.11] SD decrease	"Illumina [301,019]"	N
11/25/2008	18445777	Styrkarsdottir	29-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple Genetic Loci for Bone Mineral Density and Fractures	Bone mineral density (spine)	"5,861 individuals"	"7,925 individuals"	6q25.1	"ESR1, C6orf97"	rs1999805-C	rs1999805	0.44	2.00E-08		0.09	[0.06-0.12] SD decrease	"Illumina [301,019]"	N
11/25/2008	18369103	Walsh	25-Apr-08	Science	http://www.ncbi.nlm.nih.gov/pubmed/18369103?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia	Schizophrenia	"150 cases, 268 controls"	"83 children, 154 parents"	Pending	Pending	Pending		Pending	Pending	Pending	Pending	Pending	"Illumina [~550,000]"	Y
11/25/2008	18439552	Reiner	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein	C-reactive protein	909 individuals	"5,106 individuals"	19q13.32	APOE	rs2075650-?	rs2075650	NR	1.00E-07		NR	NR	"Illumina [317,000]"	N
11/25/2008	18439552	Reiner	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein	C-reactive protein	909 individuals	"5,106 individuals"	1q23.2	CRP	rs11265260-?	rs11265260	NR	7E-06		NR	NR	"Illumina [317,000]"	N
11/25/2008	18439552	Reiner	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein	C-reactive protein	909 individuals	"5,106 individuals"	12q24.31	HNF1A	rs1169310-A	rs1169310	0.38	2.00E-08		0.13	[0.08-0.17] mg/l decrease in log(CRP) level	"Illumina [317,000]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	12q24.31	HNF1A	rs7310409-A	rs7310409	NR	7.00E-17		0.15	[NR] mg/dl decrease	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	2p23.3	GCKR	rs780094-A	rs780094	NR	7.00E-15		0.14	[NR] mg/dl increase	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	12q23.2	Unknown	rs10778213-G	rs10778213	NR	1.00E-10		0.12	[NR] mg/dl decrease	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	1q21.3	IL6R	rs8192284-?	rs8192284	NR	2.00E-08		0.1	[NR] mg/dl decrease	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	1p31.3	LEPR	rs1892534-A	rs1892534	NR	7.00E-21		0.17	[NR] mg/dl decrease	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	1q23.2	CRP	rs3091244-?	rs3091244	NR	6.00E-28		0.2	[NR] mg/dl increase	"Illumina [336,108]"	N
11/25/2008	18439548	Ridker	24-Apr-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study"	C-reactive protein	"6,345 women"	NR	19q13.32	APOE	rs769449-?	rs769449	NR	9.00E-21		0.26	[NR] mg/dl decrease	"Illumina [336,108]"	N
11/25/2008	18403759	Ober	9-Apr-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18403759?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Effect of Variation in CHI31 on Serum YKL-40 Level, Risk of Asthma, and Lung Function"	YKL-40 levels	632 individuals	206 children	1q32.1	CHI3L1	rs4950928-G	rs4950928	0.29	1.00E-13		0.3	[NR] ng/ml decrease	"Affymetrix [290,325]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	7p22.2	GNA12	rs798544-G	rs798544	0.72	7.00E-15		5.9	[6.03-8.77] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6q24.1	GPR126	rs3748069-A	rs3748069	0.74	5.00E-14		6.5	[5.44-9.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	4q31.22	HHIP	rs1812175-C	rs1812175	0.86	1.00E-11		8.3	[5.95-10.65] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p24.3	BMP6	rs12198986-A	rs12198986	0.5	2.00E-11		6.8	[4.84-8.76] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	1q21.2	"Histone class 2A,MTMR11, SV2A, SF3B4"	rs11205277-G	rs11205277	0.44	1.00E-10		5.1	[3.53-6.67] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	1q24.3	DNM3	rs678962-G	rs678962	0.22	3.00E-08		5.4	[3.44-7.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6q21	"LIN28B, HACE1, BVES, POPDC3"	rs314268-C	rs314268	0.34	8.00E-07		4.6	[2.84-6.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6q21	"PPIL6, CD164, SMPD2,MNICAL1,ZBTB24"	rs9487094-G	rs9487094	0.69	4E-06		4.7	[2.74-6.66] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6q22.32	C6orf173	rs1490388-T	rs1490388	0.42	6.00E-07		4.8	[2.84-6.76] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6q22.33-6q23.1	"L3MBTL3, SAMD3"	rs6899976-G	rs6899976	0.28	0.000006		3.8	[2.23-5.37] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	9q22.1	"SPIN1, CCRK"	rs2814828-T	rs2814828	0.25	9.00E-07		5.4	[3.24-7.56] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	9q32	COL27A1	rs946053-T	rs946053	0.52	2.00E-07		4.4	[2.83-5.97] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	12p13.2	ETV6	rs2187642-A	rs2187642	0.39	2E-06		4.6	[2.64-6.56] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	12p12.2	"PDE3A, SLCO1C1, SLCO1B3"	rs11611208-A	rs11611208	0.06	2E-06		11.4	[6.7-16.1] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	12q15	"LYZ,YEATS4,FRS2,CPSF6,CCT2,LRRC10"	rs11177669-A	rs11177669	0.31	0.000003		4.5	[2.54-6.46] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	12q22	"SOCS2, MRPL42, CRADD, UBE2N"	rs3825199-C	rs3825199	0.24	2.00E-07		6.2	[3.85-8.55] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	13q14.3	DLEU7	rs1239947-G	rs1239947	0.35	8E-06		3.8	[2.23-5.37] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	15q25.2	"ADAMTSL3, SH3GL3"	rs2554380-T	rs2554380	0.78	9.00E-07		4.5	[2.74-6.26] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	16q24.1	"ZDHHC7, CRISPLD2, USP10"	rs2326458-C	rs2326458	0.26	8.00E-07		5.1	[3.14-7.06] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	17q23.3	"MAP3K3, WDR68, LYK5, MT1F"	rs7209435-C	rs7209435	0.27	7.00E-07		4.8	[2.84-6.76] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	19p13.2	"ADAMTS10, MYO1F, PRAM1, OR2Z1"	rs7249094-G	rs7249094	0.59	1.00E-06		4.3	[2.54-6.06] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	22q11.23	"BCR, GNAZ, RTDR1, IGLL1"	rs5751614-A	rs5751614	0.49	0.000006		4.3	[2.34-6.26] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	Xq21.1	ITM2A	rs1474563-T	rs1474563	0.58	0.000003		3.5	[1.93-5.07] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	20q11.22	"UQCC, GDF5, CEP250, EIF6, MMP24"	rs6088792-T	rs6088792	0.26	8.00E-07		4.7	[2.74-6.66] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	14q32.12	"TRIP11, FBLN5, ATXN3, CPSF2"	rs7153027-A	rs7153027	0.52	1.00E-10		5.7	[3.94-7.46] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	1q25.3	"C1orf19,GLT25D2"	rs2274432-T	rs2274432	0.37	8.00E-09		5.3	[3.54-7.06] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	2p16.1	"EFEMP1, PNPT1"	rs3791679-T	rs3791679	0.81	6.00E-11		5.8	[4.04-7.56] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	4p15.32	"LCORL, NCAPG"	rs6830062-T	rs6830062	0.89	1.00E-10		6.3	[4.34-8.26] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p22.1	"Histone class 1,Butyrophilin genes"	rs10946808-A	rs10946808	0.7	6.00E-10		5.6	[3.84-7.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p21.32	HLA class III	rs185819-T	rs185819	0.52	3.00E-08		5.2	[3.44-6.96] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p21.31	"HMGA1, LBH"	rs1776897-C	rs1776897	0.07	1.00E-08		8.8	[5.66-11.94] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p21.31	"ANKS1A, TCP11, ZNF76, DEF6,SCUBE3"	rs4713858-G	rs4713858	0.86	4.00E-08		6.8	[4.45-9.15] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	7q21.2	"CDK6, PEX1, GATAD1, ERVWE1"	rs2282978-C	rs2282978	0.29	1.00E-08		5.8	[3.84-7.76] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	8q12.1	"PLAG1, MOS, CHCHD7,RDHE2, RPS20,LYN, TGS1, PENK"	rs10958476-C	rs10958476	0.23	7.00E-08		5.4	[3.44-7.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	8q21.11	"PXMP3, ZFHX4"	rs7846385-C	rs7846385	0.27	5.00E-08		5	[3.24-6.76] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	9q31.2	ZNF462	rs4743034-A	rs4743034	0.23	2.00E-08		5.3	[3.54-7.06] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	12q14.3	HMGA2	rs8756-C	rs8756	0.52	2.00E-16		6.6	[5.03-8.17] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	15q26.3	ADAMTS17	rs4533267-A	rs4533267	0.28	3.00E-08		5.6	[3.64-7.56] % SD taller % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	17q11.2	"CRLF3, ATAD5, CENTA2, RNF135"	rs3760318-C	rs3760318	0.63	2.00E-09		6	[4.04-7.96] % SD taller % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	17q22	"NOG, DGKE, TRIM25, COIL, RISK"	rs4794665-A	rs4794665	0.48	1.00E-07		3.6	[2.23-4.97] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	17q23.2	"BCAS3, NACA2, TBX2, TBX4"	rs757608-T	rs757608	0.35	6.00E-08		4.4	[2.83-5.97] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	18q11.2	"CABLES1, RBBP8, C18orf45"	rs4800148-A	rs4800148	0.79	4.00E-09		6.4	[4.24-8.56] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	20p12.3	BMP2	rs967417-C	rs967417	0.53	2.00E-08		4.3	[2.73-5.87] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	2p23.3	"ADCY3, RBJ, POMC, DNMT3A, DTNB"	rs6733301-G	rs6733301	0.87	8.00E-07		7.5	[4.56-10.44] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	2q35	"IHH, CRYBA2, FEV, SLC23A3, TUBA1"	rs1052483-C	rs1052483	0.91	1.00E-06		6.9	[4.16-9.64] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	2q37.1	"NPPC, DIS3L2, COPS7B, PDE6D, PTMA"	rs749052-A	rs749052	0.94	1.00E-06		8.7	[5.17-12.23] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	3q26.2	"GOLIM4, SERPINI1"	rs4345115-T	rs4345115	0.63	7E-06		4.4	[2.44-6.36] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	4q21.21	"BMP3, PRKG2, RASGEF1B"	rs710841-A	rs710841	0.27	2E-06		5	[3.04-6.96] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	5q31.1	"PITX1, PCBD2, CATSPER3, TXNDC15,DDX46, CAMLG"	rs31198-T	rs31198	0.75	8E-06		4.8	[2.64-6.96] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p22.3	"NUP153, CAP2, KIF13A"	rs12199222-T	rs12199222	0.33	7.00E-07		4.4	[2.64-6.16] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	6p12.3	"SUPT3H, RUNX2"	rs9395066-C	rs9395066	0.48	8E-06		3.5	[1.93-5.07] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391951	Gudbjartsson	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Many sequence variants affecting diversity of adult human height	Height	"30,968 individuals"	"8,541 individuals"	3q23	ZBTB38	rs6763931-A	rs6763931	0.45	1.00E-27		7.4	[6.03-8.77] % SD taller	"Illumina and Affymetrix [up to 304,226]"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	14q13.3	NKX2-1	rs17104630-G	rs17104630	0.04	8E-06		0.42	[0.61-1.10] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	12q14.3	HMGA2	rs1042725-T	rs1042725	0.49	3.00E-20		0.48	[0.58-1.09] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	20q11.22	"GDF5,UQCC"	rs6060369-C	rs6060369	0.36	1.00E-16		0.44	[0.34-0.72] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	6q21	LIN28B	rs314277-A	rs314277	0.13	1.00E-08		0.41	[0.26-0.59] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	19p13.3	DOT1L	rs12986413-T	rs12986413	0.45	3.00E-08		0.31	[0.21-0.46] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	15q25.2	"SH3GL3,ADAMTSL3"	rs2562784-G	rs2562784	0.17	6.00E-08		0.34	[0.21-0.48] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	8q12.1	"CHCHD7,RDHE2"	rs9650315-T	rs9650315	0.13	4.00E-07		0.43	[0.59-1.07] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	7q21.2	CDK6	rs2040494-C	rs2040494	0.5	4.00E-07		0.26	[0.36-0.65] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	7q36.3	WDR60	rs2730245-G	rs2730245	0.33	3.00E-07		0.32	[0.19-0.44] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	9q34.11	FUBP3	rs7466269-G	rs7466269	0.33	8.00E-07		0.27	[0.38-0.69] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	9q33.1	PAPPA	rs7869550-G	rs7869550	0.24	1.00E-06		0.33	[0.45-0.82] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	3q23	ZBTB38	rs724016-G	rs724016	0.48	8.00E-22		0.37	[0.29-0.45] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	6q24.3	GPR126	rs4896582-A	rs4896582	0.27	2.00E-18		0.38	[0.28-0.48] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	6q22.1	HIST1H1D	rs10946808-G	rs10946808	0.28	4.00E-17		0.36	[0.26-0.46] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	4q31.22	HHIP	rs1492820-G	rs1492820	0.48	1.00E-11		0.29	[0.21-0.37] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	14q32.12	"TRIP11,ATXN3"	rs8007661-T	rs8007661	0.3	6.00E-10		0.42	[0.30-0.54] cm shorter	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	17q22	ANKFN1	rs12449568-C	rs12449568	0.47	2E-06		0.25	[0.15-0.35] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391950	Lettre	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ten loci associated with height highlights new biological pathways in human growth	Height	"15,821 individuals"	"13,671 individuals"	16p13.3	RAB40C	rs763014-C	rs763014	0.43	0.000005		0.24	[0.12-0.29] cm taller	"Affymetrix and Illumina [2,260,683] (imputed)"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	15q25.2	ADAMTSL3	rs10906982-A	rs10906982	0.48	2.00E-08		0.05	[0.02-0.07] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	13q14.3	DLEU7	rs3116602-G	rs3116602	0.21	7.00E-09		0.04	[0.00-0.07] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	1q42.13	ZNF678	rs1390401-A	rs1390401	0.18	5.00E-09		0.04	[0.01-0.08] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	4q31.22	HHIP	rs6854783-A	rs6854783	0.43	2.00E-09		0.06	[0.03-0.08] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	12q22	SOCS2	rs11107116-G	rs11107116	0.23	6.00E-10		0.04	[0.01-0.07] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	1p12	SPAG17	rs12735613-A	rs12735613	0.24	4.00E-11		0.08	[0.05-0.11] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	9q22.32	PTCH1	rs10512248-G	rs10512248	0.31	4.00E-11		0.05	[0.02-0.07] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	6p21.31	C6orf106	rs2814993-A	rs2814993	0.15	4.00E-12		0.09	[0.05-0.13] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	3q23	ZBTB38	rs6440003-A	rs6440003	0.44	2.00E-24		0.07	[0.04-0.09] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	7q21.2	CDK6	rs2282978-C	rs2282978	0.33	8.00E-23		0.09	[0.06-0.12] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	12q14.3	HMGA2	rs1042725-C	rs1042725	0.49	3.00E-18		0.05	[0.03-0.08] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	20q11.22	GDF5	rs6060373-G	rs6060373	0.38	2.00E-17		0.08	[0.05-0.11] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	4p15.32	LCORL	rs16896068-A	rs16896068	0.16	2.00E-13		0.07	[0.03-0.11] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	1p34.2	SCMH1	rs6686842-C	rs6686842	0.44	2.00E-08		0.05	[0.02-0.08] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	2q35	IHH	rs6724465-A	rs6724465	0.1	2.00E-08		0.06	[0.02-0.10] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	3q22.2	"ANAPC13,CEP63"	rs10935120-A	rs10935120	0.33	7.00E-08		0.06	[0.03-0.09] SD shorter - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	15q26.1	ACAN	rs8041863-A	rs8041863	0.47	8.00E-08		0.04	[0.01-0.06] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	18q21.1	DYM	rs8099594-A	rs8099594	0.35	3.00E-07		0.05	[0.02-0.08] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	6q22.32	LOC387103	rs4549631-C	rs4549631	0.5	5.00E-13		0.06	[0.03-0.08] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18391952	Weedon	6-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies 20 loci that influence adult height	Height	"13,665 individuals"	"16,482 individuals"	2p16.1	EFEMP1	rs3791675-C	rs3791675	0.23	2.00E-12		0.09	[0.05-0.12] SD taller - among males	"Affymetrix [402,951]"	N
11/25/2008	18369459	Liu	4-Apr-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci	Psoriasis	"218 cases, 519 controls"	"1,153 cases, 1,217 controls"	13q13	COG6	rs7993214-?	rs7993214	0.65	2E-06		1.41	[1.22-1.61]	"Illumina [305,983]"	N
11/25/2008	18369459	Liu	4-Apr-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci	Psoriasis	"218 cases, 519 controls"	"1,153 cases, 1,217 controls"	6p21.33	HLA-C	rs2395029-C	rs2395029	0.03	2.00E-26		4.1	[3.10-5.30]	"Illumina [305,983]"	N
11/25/2008	18369459	Liu	4-Apr-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci	Psoriasis	"218 cases, 519 controls"	"1,153 cases, 1,217 controls"	6p21.33	HLA-C	rs10484554-T	rs10484554	0.15	2.00E-39		2.8	[2.40-3.30]	"Illumina [305,983]"	N
11/25/2008	18385676	Amos	3-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1	Lung cancer	"1,154 cases, 1,137 controls"	"2,724 cases, 3,694 controls"	3q28	IL1RAP	rs7626795-G	rs7626795	NR	8E-06		1.16	[1.05-1.28]	"Illumina [317,498]"	N
11/25/2008	18385676	Amos	3-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1	Lung cancer	"1,154 cases, 1,137 controls"	"2,724 cases, 3,694 controls"	1q23.2	CRP	rs2808630-G	rs2808630	NR	7E-06		1.22	[1.10-1.35]	"Illumina [317,498]"	N
11/25/2008	18385676	Amos	3-Apr-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1	Lung cancer	"1,154 cases, 1,137 controls"	"2,724 cases, 3,694 controls"	15q25.1	"CHRNA3, CHRNA5, PSMA4, LOC123688"	rs8034191-G	rs8034191	NR	3.00E-18		1.3	[1.15-1.47]	"Illumina [317,498]"	N
11/25/2008	18385738	Hung	3-Apr-08	Nature	http://www.ncbi.nlm.nih.gov/pubmed/18385738?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A susceptibility locus for lung cancer maps to nicotinic acteylcholine receptor subunit genes on 15q25	Lung cancer	"1,926 cases, 2,522 controls"	"2,513 cases, 4,752 controls"	15q25.1	"CHRNA3,CHRNA5, CHRNB4, PSMA4, LOC123688"	rs8034191-C	rs8034191	0.34	5.00E-20		1.3	[1.23-1.37]	"Illumina [310,023]"	N
11/25/2008	18385739	Thorgeirsson	3-Apr-08	Nature	http://www.ncbi.nlm.nih.gov/pubmed/18385739?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"A variant associated with nicotine dependence, lung cancer and peripheral arterial disease"	Nicotine dependence	"10,995 smokers"	"4,848 smokers"	15q25.1	"CHRNA3,CHRNA5,CHRNB4"	rs1051730-T	rs1051730	0.35	6.00E-20		0.1	[0.08-0.12] increase in cigarettes per day	"Illumina [306,207]"	N
11/25/2008	18372901	Tenesa	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21	Colorectal cancer	"981 cases, 1,002 controls"	"16,476 cases, 15,351 controls"	8q24.21	"POU5FIP1, HsG57825, DQ515897"	rs7014346-A	rs7014346	0.18	9.00E-26		1.19	[1.15-1.23]	"Illumina [541,628]"	N
11/25/2008	18372901	Tenesa	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21	Colorectal cancer	"981 cases, 1,002 controls"	"16,476 cases, 15,351 controls"	11q23.1	Intergenic	rs3802842-C	rs3802842	0.43	6.00E-10		1.11	[1.08-1.15]	"Illumina [541,628]"	N
11/25/2008	18372901	Tenesa	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21	Colorectal cancer	"981 cases, 1,002 controls"	"16,476 cases, 15,351 controls"	18q21.1	SMAD7	rs4939827-T	rs4939827	0.17	8.00E-28		1.2	[1.16-1.24]	"Illumina [541,628]"	N
11/25/2008	18372905	Tomlinson	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3	Colorectal cancer	"922 cases, 927 controls"	"17,872 cases, 17,526 controls"	10p14	Intergenic	rs10795668-A	rs10795668	0.67	3.00E-13		1.12	[1.10-1.16]	"Illumina [547,647]"	N
11/25/2008	18372905	Tomlinson	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3	Colorectal cancer	"922 cases, 927 controls"	"17,872 cases, 17,526 controls"	15q13.3	Intergenic	rs4779584-?	rs4779584	0.19	5.00E-07		1.23	[1.14-1.34]	"Illumina [547,647]"	N
11/25/2008	18372905	Tomlinson	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3	Colorectal cancer	"922 cases, 927 controls"	"17,872 cases, 17,526 controls"	18q21.1	SMAD7	rs4939827-?	rs4939827	0.53	2E-06		1.18	[1.10-1.25]	"Illumina [547,647]"	N
11/25/2008	18372905	Tomlinson	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3	Colorectal cancer	"922 cases, 927 controls"	"17,872 cases, 17,526 controls"	8q24.21	Intergenic	rs6983267-?	rs6983267	0.48	7.00E-11		1.24	[1.17-1.33]	"Illumina [547,647]"	N
11/25/2008	18372905	Tomlinson	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3	Colorectal cancer	"922 cases, 927 controls"	"17,872 cases, 17,526 controls"	8q23.3	EIF3H	rs16892766-A	rs16892766	0.07	3.00E-18		1.27	[1.20-1.34]	"Illumina [547,647]"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	10q23.33	HHEX	rs5015480-C	rs5015480	NR	7.00E-08		1.17	[1.11-1.24]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	9p21.3	"CDKN2A,CDKN2B"	rs7020996-C	rs7020996	NR	2.00E-07		1.26	[1.15-1.38]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	1p12	"NOTCH2, ADAM30"	rs10923931-T	rs10923931	0.11	4.00E-08		1.13	[1.08-1.17]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	12q13.2	DCD	rs1153188-A	rs1153188	0.73	2.00E-07		1.08	[1.05-1.11]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	6p21.1	VEGFA	rs9472138-T	rs9472138	0.28	4E-06		1.06	[1.04-1.09]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	3p25.2	"SYN2, PPARG"	rs17036101-G	rs17036101	0.93	2.00E-07		1.15	[1.10-1.21]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	3q27.2	IGF2BP2	rs4402960-T	rs4402960	NR	8.00E-08		1.17	[1.10-1.25]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	11p15.1	KCNJ11	rs5215-C	rs5215	NR	4.00E-07		1.16	[1.09-1.23]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	10q25.2	TCF7L2	rs7903146-T	rs7903146	NR	3.00E-23		1.37	[1.28-1.47]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	16q12.2	FTO	rs8050136-A	rs8050136	NR	7E-06		1.15	[1.09-1.22]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	7p15.1	JAZF1	rs864745-T	rs864745	0.5	5.00E-14		1.1	[1.07-1.13]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	10p13	"CDC123,CAMK1D"	rs12779790-G	rs12779790	0.18	1.00E-10		1.11	[1.07-1.14]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	12q21.1	"TSPAN8,LGR5"	rs7961581-C	rs7961581	0.27	1.00E-09		1.09	[1.06-1.12]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	6p22.3	CDKAL1	rs6931514-G	rs6931514	NR	1.00E-11		1.25	[1.17-1.33]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	3p14.1	ADAMTS9	rs4607103-C	rs4607103	0.76	1.00E-08		1.09	[1.06-1.12]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18372903	Zeggini	30-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes	Type 2 diabetes	"4,549 cases, 5,579 controls"	"24,194 cases, 55,598 controls"	2p21	THADA	rs7578597-T	rs7578597	0.9	1.00E-09		1.15	[1.10-1.20]	"Affymetrix and Illumina [2,202,892] (imputed)"	N
11/25/2008	18360741	Butcher	25-Mar-08	Behav Genet	http://www.ncbi.nlm.nih.gov/pubmed/18360741?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	The Nature of Nuture: A Genomewide Association Scan for Family Chaos	Environmental confusion in the home	"469 children from low chaos families,369 children from high chaos families"	"3,529 children"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [117,062] (pooled)"	N
11/25/2008	18364390	Capon	25-Mar-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/18364390?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene	Psoriasis	"318 cases, 288 controls"	"2,361 cases, 1,927 controls"	6p21.33	HLA-C	rs3134792-?	rs3134792	NR	1.00E-09		NR	NR	"Illumina [~408,000] (pooled)"	N
11/25/2008	18364390	Capon	25-Mar-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/18364390?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene	Psoriasis	"318 cases, 288 controls"	"2,361 cases, 1,927 controls"	20q13.13	SPATA2	rs495337-?	rs495337	NR	1.00E-08		1.25	[1.12-1.39]	"Illumina [~408,000] (pooled)"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	13q12.2	Intergenic	rs9512730-?	rs9512730	0.26	0.000005		1.52	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	15q25.3	AGBL1	rs16977195-?	rs16977195	0.03	2E-06		6.01	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	1q31.1	Intergenic	rs10911902-?	rs10911902	0.17	2E-06		1.79	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	1p36.22	Intergenic	rs4846033-?	rs4846033	0.01	4E-06		2.87	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	16p12.2	"ACSM1, BUCS1"	rs151222-?	rs151222	0.08	0.000006		2.1	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18347602	Sullivan	18-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Genomewide association for schizophrenia in the CATIE study: results of stage 1	Schizophrenia	"738 cases, 733 controls"	NR	Xq28	Intergenic	rs2159767-?	rs2159767	0.62	7E-06		1.33	[NR]	"Affymetrix [492,900]"	N
11/25/2008	18326623	Gold	11-Mar-08	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/18326623?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33	Breast cancer	"249 cases, 299 controls (Ashkenazi Jewish, non-BRCA1/2 carriers)"	"1,193 cases, 1,166 controls (Ashkenazi Jewish, non-BRCA1/2 carriers)"	6q22.33	"ECHDC1,RNF146"	rs2180341-G	rs2180341	0.21	3.00E-08		1.41	[1.25-1.59]	"Affymetrix [150,080]"	N
11/25/2008	18332876	Kirov	11-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18332876?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study in 574 schizophrenia trios using DNA pooling	Schizophrenia	"574 cases, 605 controls, 1,148 parents of cases"	NR	12q24.23	CCDC60	rs11064768-A	rs11064768	0.91	1.00E-06		NR	NR	"Illumina [~550,000] (pooled)"	N
11/25/2008	18327256	Doring	9-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18327256?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	SLC2A9 influences uric acid concentrations with pronounced sex-specific effects	Serum urate	"1,644 individuals"	"9,947 individuals"	4p16.1	SLC2A9	rs7442295-C	rs7442295	0.4	3.00E-70		0.35	[NR] mg/dl decrease in uric acid	"Affymetrix [335,152]"	N
11/25/2008	18327257	Vitart	9-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18327257?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout"	Serum urate	794 individuals	706 individuals	4p16.1	SLC2A9	rs737267-C	rs737267	0.31	3.00E-09		0.88	[NR] uM decrease in uric acid [females only]	"Illumina [308,140]"	N
11/25/2008	18325910	Liu	5-Mar-08	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/18325910?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scans identified CTNNBL1 as a novel gene for obesity	Obesity	"1,000 individuals"	"896 obese individuals, 2,916 lean individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [379,319]"	N
11/25/2008	18317468	Sklar	4-Mar-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18317468?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole-genome association study of bipolar disorder	Bipolar disorder	"1,461 cases, 2,008 controls"	"409 trios, 365 cases, 351 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [372,193]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	6q25.3	TAGAP	rs1738074-A	rs1738074	NR	7.00E-08		1.21	[1.13-1.30]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	4q27	"KIAA1109, ADAD1, IL2, IL21"	rs6822844-C	rs6822844	0.81	3.00E-13		1.44	[1.30-1.58]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	12q24.12	"SH2B3, ATXN2"	rs653178-G	rs653178	0.48	8.00E-08		1.21	[1.13-1.30]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	3p21.31	"CCR1, CCR3"	rs6441961-A	rs6441961	0.3	3.00E-07		1.21	[1.13-1.30]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	1q31.2	RGS1	rs2816316-C	rs2816316	NR	3.00E-11		1.39	[1.26-1.53]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	2q12.1	"IL1RL1,IL18R1,IL18RAP, SLC9A4"	rs13015714-C	rs13015714	NR	4.00E-09		1.28	[1.18-1.39]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	3q25.33	"IL12A, SCHIP1"	rs17810546-G	rs17810546	NR	1.00E-09		1.35	[1.23-1.49]	"Illumina [310,605]"	N
11/25/2008	18311140	Hunt	2-Mar-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified genetic risk variants for celiac disease related to the immune response	Celiac disease	"767 cases, 1,422 controls"	"1,643 cases, 3,406 controls"	3q28	LPP	rs1464510-A	rs1464510	NR	5.00E-09		1.23	[1.15-1.32]	"Illumina [310,605]"	N
11/25/2008	18316681	Uhl	1-Mar-08	Arch Gen Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18316681?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association for methamphetamine dependence: convergent results from 2 samples	Methamphetamine dependence	"240 cases, 340 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [up to 466,883] (pooled)"	N
11/25/2008	18313986	Blauw	29-Feb-08	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/18313986?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen	Amyotrophic lateral sclerosis	"406 cases, 404 controls"	NR	Pending	Pending	Pending		Pending	Pending	Pending	Pending	Pending	"Illumina [317,503]"	Y
11/25/2008	18282107	Shifman	15-Feb-08	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/18282107?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women	Schizophrenia	"660 cases, 2,271 controls"	"2,274 cases, 4,401 controls"	7q22.1	RELN	rs7341475-G	rs7341475	0.62	9.00E-07		1.58	[1.31-1.89]	"Affymetrix [510,552]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	8q24.21	Intergenic	rs6983267-G	rs6983267	0.49	9.00E-13		1.42	[NR]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	8q24.21	Intergenic	rs1016343-T	rs1016343	0.18	1.00E-07		1.37	[NR]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	8q24.21	Intergenic	rs4242384-C	rs4242384	0.09	3.00E-16		1.88	[NR]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	17q12	HNF1B	rs7501939-C	rs7501939	0.57	9.00E-12		1.41	[NR]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	17q24.3	Intergenic	rs1859962-G	rs1859962	0.46	1.00E-06		1.26	[NR]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	Xp11.22	"NUDT10, NUDT11"	rs5945619-C	rs5945619	0.36	2.00E-09		1.19	[1.07-1.31]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	3p12.1	SLC22A3	rs2660753-T	rs2660753	0.11	3.00E-08		1.18	[1.06-1.31]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	10q11.23	MSMB	rs10993994-T	rs10993994	0.4	9.00E-29		1.25	[1.17-1.34]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	7q21.3	LMTK2	rs6465657-C	rs6465657	0.46	1.00E-09		1.12	[1.05-1.20]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	6q25.3	SLC22A3	rs9364554-T	rs9364554	0.29	6.00E-10		1.17	[1.08-1.26]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	11q13.2	Intergenic	rs7931342-G	rs7931342	0.51	2.00E-12		1.19	[1.11-1.27]	"Illumina [541,129]"	N
11/25/2008	18264097	Eeles	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple newly identified loci associated with prostate cancer susceptibility	Prostate cancer	"1,854 cases, 1,894 controls"	"3,268 cases, 3,366 controls"	19q13.33	KLK3	rs2735839-G	rs2735839	0.85	2.00E-18		1.2	[1.10-1.33]	"Illumina [541,129]"	N
11/25/2008	18264098	Gudmundsson	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264098?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer	Prostate cancer	"1,854 cases, 21,372 controls"	"8,239 cases, 7,590 controls"	2p15	EHBP1	rs721048-A	rs721048	0.19	8.00E-09		1.15	[1.10-1.21]	"Illumina [310,520]"	N
11/25/2008	18264098	Gudmundsson	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264098?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer	Prostate cancer	"1,854 cases, 21,372 controls"	"8,239 cases, 7,590 controls"	Xp11.22	"NUDT10, NUDT11, LOC340602, GSPT2, MAGED1"	rs5945572-A	rs5945572	0.35	4.00E-13		1.23	[1.16-1.30]	"Illumina [310,520]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	10q11.23	MSMB	rs10993994-T	rs10993994	0.4	7.00E-13		1.16	[1.04-1.29]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	8q24.21	Intergenic	rs4242382-A	rs4242382	0.12	3.00E-19		1.66	[1.47-1.87]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	17q12	HNF1B	rs4430796-A	rs4430796	0.54	1.00E-09		1.18	[1.04-1.32]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	7p15.2	JAZF1	rs10486567-G	rs10486567	0.77	2E-06		1.12	[1.02-1.25]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	11q13.2	Intergenic	rs10896449-G	rs10896449	0.52	2.00E-09		1.1	[0.98-1.23]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	10q26.13	CTBP2	rs4962416-C	rs4962416	0.27	2.00E-07		1.17	[1.05-1.30]	"Illumina [527,869]"	N
11/25/2008	18264096	Thomas	10-Feb-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Multiple loci identified in a genome-wide association study of prostate cancer	Prostate cancer	"1,172 cases, 1,157 controls"	"3,941 cases, 3,964 controls"	8q24.21	Intergenic	rs6983267-G	rs6983267	0.53	7.00E-12		1.28	[1.15-1.45]	"Illumina [527,869]"	N
11/25/2008	18262040	Sandhu	9-Feb-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	LDL-cholesterol concentrations: a genome-wide association study	LDL cholesterol	"11,685 individuals"	"5,036 individuals"	19q13.32	APOC1	rs4420638-G	rs4420638	0.18	1.00E-20		0.06	[0.04-0.08] mmol/L increase	"Affymetrix and Illumina [up to 461,986]"	N
11/25/2008	18262040	Sandhu	9-Feb-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	LDL-cholesterol concentrations: a genome-wide association study	LDL cholesterol	"11,685 individuals"	"5,036 individuals"	2p24.1	APOB	rs562338-T	rs562338	0.2	1.00E-09		0.04	[0.02-0.06] mmol/L decrease	"Affymetrix and Illumina [up to 461,986]"	N
11/25/2008	18262040	Sandhu	9-Feb-08	Lancet	http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	LDL-cholesterol concentrations: a genome-wide association study	LDL cholesterol	"11,685 individuals"	"5,036 individuals"	1p13.3	"CELSR2,PSRC1"	rs599839-G	rs599839	0.19	1.00E-33		0.16	[0.14-0.18] mmol/L decrease	"Affymetrix and Illumina [up to 461,986]"	N
11/25/2008	18245381	Uda	5-Feb-08	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/18245381?rdinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia	Fetal hemoglobin levels	"4,305 individuals"	521 individuals	2p15	BCL11A	rs1186868-T	rs1186868	0.2	7.00E-35		0.48	[NR] SD decrease in HbF	"Affymetrix [362,129]"	N
11/25/2008	18245381	Uda	5-Feb-08	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/18245381?rdinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia	Fetal hemoglobin levels	"4,305 individuals"	521 individuals	11p15.4	HBB	rs4910742-A	rs4910742	0.07	1.00E-21		0.58	[NR] SD decrease in HbF	"Affymetrix [362,129]"	N
11/25/2008	18239089	Kong	2-Feb-08	Science	http://www.ncbi.nlm.nih.gov/pubmed/18239089?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence Variants in the RNF212 Gene Associate with Genomewide Recombination Rate	Recombination rate (females)	"1,702 women"	"1,663 women"	4p16.3	"RNF212,SPON2"	rs1670533-C	rs1670533	0.23 (men and women combined)	2.00E-12		88.2	[63.7-112.7] cM increase	"Illumina [309,241]"	N
11/25/2008	18239089	Kong	2-Feb-08	Science	http://www.ncbi.nlm.nih.gov/pubmed/18239089?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence Variants in the RNF212 Gene Associate with Genomewide Recombination Rate	Recombination rate (males)	"1,887 men"	"1,248 men"	4p16.3	"RNF212,SPON2"	rs3796619-T	rs3796619	0.33 (men and women combined)	3.00E-24		70.7	[84.3-57.1] cM decrease	"Illumina [309,241]"	N
12/11/2008	18227835	Berrettini	29-Jan-08	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/18227835?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum	Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking	Nicotine dependence	"7,481 individuals"	~2000 individuals	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [460,959]"	N
11/25/2008	18252221	Kayser	24-Jan-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18252221?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene	Iris color	"1,406 individuals"	"8,273 individuals"	15q13.1	HERC2	rs916977-?	rs916977	NR	1.00E-43		NR	NR	"Affymetrix and Illumina [up to ~500,000] (pooled)"	N
11/25/2008	18067574	Butcher	22-Jan-08	Genes Brain Behav	http://www.ncbi.nlm.nih.gov/pubmed/18067574?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays	General cognitive ability	"458 low g, 402 high g twin children (unrelated)"	"3,195 twin children (unrelated)"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [449,127]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	16p11.2	ITGAM	rs9888739-T	rs9888739	0.13	2.00E-23		1.62	[1.47-1.78]	"Illumina [317,501]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	6p21.33	HLA region	rs3131379-A	rs3131379	0.1	2.00E-52		2.36	[2.11-2.64]	"Illumina [317,501]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	3p14.3	PXK	rs6445975-C	rs6445975	0.28	7.00E-09		1.25	[1.16-1.35]	"Illumina [317,501]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	1q25.1	Intergenic	rs10798269-?	rs10798269	0.64	1.00E-07		1.22	[1.14-1.32]	"Illumina [317,501]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	11p15.5	KIAA1542	rs4963128-?	rs4963128	0.34	3.00E-10		1.28	[1.18-1.37]	"Illumina [317,501]"	N
11/25/2008	18204446	Harley	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci"	Systemic lupus erythematosus	"720 female cases, 2,337 female controls"	"1,846 female cases, 1,825 female controls"	7q32.1	"IRF5, TNPO3"	rs12537284-A	rs12537284	0.13	4.00E-19		1.54	[1.40-1.70]	"Illumina [317,501]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	1p31.3	NEGR1	rs12141391-A	rs12141391	0.02	7E-06		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	9q34.13	NTNG2	rs11243676-A	rs11243676	0.07	0.000003		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	5p12	GHR	rs979233-T	rs979233	0.46	4E-06		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	18q22.3	SOCS6	rs17083844-A	rs17083844	0.03	0.000006		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	8p23.1	"C8orf13, BLK"	rs13277113-A	rs13277113	0.23	1.00E-10		1.39	[1.28-1.51]	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	6p21.32	HLA-DQA1	rs2187668-A	rs2187668	0.11	3.00E-21		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	7q32.1	"IRF5, TNPO3"	rs10488631-C	rs10488631	0.12	2.00E-11		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	2q32.3	STAT4	rs7574865-T	rs7574865	0.23	9.00E-14		NR	NR	"Illumina [502,033]"	N
11/25/2008	18204098	Hom	20-Jan-08	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX	Systemic lupus erythematosus	"1,311 cases, 3,340 controls"	"793 cases, 857 controls"	16p11.2	"ITGAM, ITGAX"	rs11574637-C	rs11574637	0.19	3.00E-11		1.33	[1.22-1.46]	"Illumina [502,033]"	N
11/25/2008	18204447	Kozyrev	20-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18204447?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus	Systemic lupus erythematosus	"279 cases, 515 controls"	"1,757 cases, 1,540 controls"	4q24	BANK1	rs10516487-G	rs10516487	0.77	4.00E-10		1.38	[1.25-1.53]	"Affymetrix [85,042]"	N
11/25/2008	18198356	Hakonarson	15-Jan-08	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/18198356?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study	Type 1 diabetes	"467 trios, 561 cases, 1,143 controls"	"549 families, 364 trios"	12q13.2	"RAB5B, SUOX, IKZF4, ERBB3, CDK2"	rs1701704-C	rs1701704	0.35	9.00E-10		1.25	[1.12-1.40]	"Illumina [543,071]"	N
11/25/2008	18195134	Byun	14-Jan-08	Arch Neurol	http://www.ncbi.nlm.nih.gov/pubmed/18195134?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-Wide Pharmacogenomic Analysis of the Response to Interferon Beta Therapy in Multiple Sclerosis	Response to interferon beta therapy	206 multiple sclerosis cases	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~100,000] (pooled)"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	8p21.3	LPL	rs328-G	rs328	0.09	9.00E-23		0.17	[0.13-0.21]% SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	1q42.13	GALNT2	rs4846914-G	rs4846914	0.4	2.00E-13		0.07	[0.05-0.09] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	9q31.1	ABCA1	rs3890182-A	rs3890182	0.13	3.00E-10		0.1	[0.06-0.14]% SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	16q13	CETP	rs1800775-C	rs1800775	0.51	1.00E-73		0.18	[0.16-0.20]% SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	18q21.1	"LIPG, ACAA2"	rs2156552-A	rs2156552	0.18	2.00E-07		0.07	[0.05-0.09]% SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	HDL cholesterol	"2,758 individuals"	"18,544 individuals"	15q22.1	LIPC	rs1800588-T	rs1800588	0.21	2.00E-32		0.14	[0.12-0.16]% SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	1p32.3	PCSK9	rs11591147-T	rs11591147	0.01	2.00E-44		0.47	[0.41-0.53] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	19p13.2	LDLR	rs6511720-T	rs6511720	0.1	2.00E-51		0.26	[0.22-0.30] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	5q13.3	HMGCR	rs12654264-T	rs12654264	0.39	1.00E-20		0.1	[0.08-0.12] % SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	19p13.11	"CILP2, PBX4"	rs16996148-T	rs16996148	0.1	3.00E-08		0.1	[0.06-0.14] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	1p13.3	"CELSR2,PSRC1,SORT1"	rs646776-C	rs646776	0.24	3.00E-29		0.16	[0.14-0.18] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	2p24.1	APOB	rs693-A	rs693	0.48	1.00E-21		0.12	[0.10-0.14] % SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	LDL cholesterol	"2,758 individuals"	"18,544 individuals"	19q13.32	"APOE, APOC1, APOC4, APOC2"	rs4420638-G	rs4420638	0.2	1.00E-60		0.19	[0.15-0.23] % SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	8q24.13	TRIB1	rs17321515-G	rs17321515	0.49	4.00E-17		0.08	[0.06-0.10] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	7q11.23	"BCL7B, TBL2, MLXIPL"	rs17145738-T	rs17145738	0.13	7.00E-22		0.14	[0.25-0.53] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	11q23.3	"APOA1, APOC3, APOA4, APOA5, ZNF259, BUD13"	rs28927680-G	rs28927680	0.07	2.00E-17		0.26	[0.20-0.32]% SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	2p24.1	APOB	rs693-A	rs693	0.48	2.00E-07		0.08	[0.04-0.12]% SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	1p31.3	"ANGPTL3, DOCK7, ATG4C"	rs12130333-T	rs12130333	0.22	2.00E-08		0.11	[0.07-0.15] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	8p21.3	LPL	rs328-G	rs328	0.09	2.00E-28		0.19	[0.15-0.23]% SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	1q42.13	GALNT2	rs4846914-G	rs4846914	0.4	7.00E-15		0.08	[0.06-0.10] % SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	19p13.11	"CILP2, PBX4"	rs16996148-T	rs16996148	0.1	4.00E-09		0.1	[0.06-0.14] % SD lower	"Affymetrix [389,878]"	N
11/25/2008	18193044	Kathiresan	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans"	Triglycerides	"2,758 individuals"	"18,544 individuals"	2p23.3	GCKR	rs780094-T	rs780094	0.34	3.00E-14		0.13	[0.09-0.17]% SD higher	"Affymetrix [389,878]"	N
11/25/2008	18193046	Kooner	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides	Triglycerides	"2,011 individuals"	"10,536 individuals"	8p21.3	"LPL, C8orf35, SLC18A1"	rs326-A	rs326	0.78	5.00E-12		6.6	[3.66-9.54] % higher	"Perlegen [up to 216,774]"	N
11/25/2008	18193046	Kooner	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides	Triglycerides	"2,011 individuals"	"10,536 individuals"	11q23.3	"APOA1,KIAA0999,LOC645044"	rs2075292-G	rs2075292	0.24	5.00E-08		8.7	[5.76-11.64] % higher	"Perlegen [up to 216,774]"	N
11/25/2008	18193046	Kooner	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides	Triglycerides	"2,011 individuals"	"10,536 individuals"	11q23.3	"LOC440069, MGC13125"	rs1558861-C	rs1558861	0.18	2.00E-26		17	[13.28-20.72] % higher	"Perlegen [up to 216,774]"	N
11/25/2008	18193046	Kooner	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides	Triglycerides	"2,011 individuals"	"10,536 individuals"	7q11.23	MLXIPL	rs3812316-C	rs3812316	0.95	1.00E-10		10.5	[5.3-17.7]% higher	"Perlegen [up to 216,774]"	N
11/25/2008	18193045	Sanna	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants in the GDF5-UQCC region are associated with variation in human height	Height	"6,669 individuals"	"28,801 individuals"	5q14.1	HOMER1	rs10078095-C	rs10078095	0.22	0.000003		0.9	[NR] cm taller	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193045	Sanna	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants in the GDF5-UQCC region are associated with variation in human height	Height	"6,669 individuals"	"28,801 individuals"	20q11.22	BFZB	rs6060369-C	rs6060369	0.44	2.00E-16		0.44	[NR] cm taller	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193045	Sanna	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants in the GDF5-UQCC region are associated with variation in human height	Height	"6,669 individuals"	"28,801 individuals"	4q12	PDGFRA	rs17690232-C	rs17690232	0.8	4.00E-07		0.86	[NR] cm taller	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193045	Sanna	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants in the GDF5-UQCC region are associated with variation in human height	Height	"6,669 individuals"	"28,801 individuals"	15q26.1	POLG	rs4932217-A	rs4932217	0.58	8.00E-07		0.66	[NR] cm taller	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193045	Sanna	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants in the GDF5-UQCC region are associated with variation in human height	Height	"6,669 individuals"	"28,801 individuals"	3q23	ZBTB38	rs724016-G	rs724016	0.36	1.00E-06		0.61	[NR] cm taller	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	16q13	CETP	rs9989419-G	rs9989419	0.65	3.00E-31		1.72	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	16q13	CETP	rs1864163-G	rs1864163	0.8	7.00E-39		4.12	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	1q42.13	GALNT2	rs2144300-T	rs2144300	0.6	3.00E-14		1.11	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	18q21.1	LIPG	rs2156552-T	rs2156552	0.84	6.00E-12		1.2	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	9q31.1	ABCA1	rs4149268-C	rs4149268	0.64	1.00E-10		0.82	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	15q22.1	LIPC	rs4775041-C	rs4775041	0.33	3.00E-20		1.38	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	8p21.3	LPL	rs10503669-A	rs10503669	0.1	4.00E-19		2.09	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	12q24.11	"MVK,MMAB"	rs2338104-G	rs2338104	0.45	3.00E-08		0.48	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	16q22.1	LCAT	rs255052-A	rs255052	0.17	1.00E-07		0.74	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	HDL cholesterol	"8,656 individuals"	"11,399 individuals"	16q13	CETP	rs3764261-A	rs3764261	0.31	2.00E-57		3.47	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	19p13.11	"NCAN,CILP2"	rs16996148-G	rs16996148	0.89	3.00E-09		3.32	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	2p24.1	APOB	rs562338-G	rs562338	0.82	6.00E-22		4.89	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	19q13.32	"APOE,APOC1,APOC4"	rs4420638-G	rs4420638	0.18	3.00E-43		6.61	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	1p32.3	PCSK9	rs11206510-T	rs11206510	0.81	4.00E-11		3.04	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	19p13.2	LDLR	rs6511720-G	rs6511720	0.9	4.00E-26		9.17	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	6p21.32	B3GALT4	rs2254287-G	rs2254287	0.38	5.00E-08		1.91	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	LDL cholesterol	"8,589 individuals"	"7,440-10,783 individuals"	1p13.3	"CELSR2,PSRC1,SORT1"	rs599839-A	rs599839	0.77	6.00E-33		5.48	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	15q22.1	LIPC	rs4775041-C	rs4775041	0.33	2.00E-08		3.62	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	19p13.3	"NCAN,CILP2"	rs16996148-G	rs16996148	0.92	3.00E-09		6.1	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	7q11.23	MLXIPL	rs17145738-C	rs17145738	0.84	2.00E-12		8.21	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	1p31.3	ANGPTL3	rs1748195-C	rs1748195	0.7	2.00E-10		7.12	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	1q42.13	GALNT2	rs2144300-C	rs2144300	0.4	8.00E-07		4.25	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	8q24.13	TRIB1	rs17321515-A	rs17321515	0.56	7.00E-13		6.42	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	11q23.3	"APOA5, APOA4, APOC3, APOA1"	rs12286037-T	rs12286037	0.06	1.00E-26		25.82	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	8p21.3	LPL	rs10503669-C	rs10503669	0.9	4.00E-22		11.57	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18193043	Willer	13-Jan-08	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Newly identified loci that influence lipid concentrations and risk of coronary artery disease	Triglycerides	"8,684 individuals"	"5,312-9,707 individuals"	2p23.3	GCKR	rs780094-T	rs780094	0.39	6.00E-32		8.59	[NR] mg/dl higher	"Illumina and Affymetrix [~2,261,000]] (imputed)"	N
11/25/2008	18179892	Wallace	10-Jan-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia	LDL cholesterol	"1,955 hypertensive individuals"	"2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)"	11q23.3	"APOA1,APOC3,APOA5"	rs6589566-G	rs6589566	0.06	3.00E-11		NR	NR	"Affymetrix [400,496]"	N
11/25/2008	18179892	Wallace	10-Jan-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia	LDL cholesterol	"1,955 hypertensive individuals"	"2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)"	2p23.3	GCKR	rs780094-T	rs780094	0.39	5.00E-07		NR	NR	"Affymetrix [400,496]"	N
11/25/2008	18179892	Wallace	10-Jan-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia	LDL cholesterol	"1,955 hypertensive individuals"	"2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)"	1p13.3	"CELSR2,PSRC1"	rs599839-G	rs599839	0.24	1.00E-07		0.95	[0.93-0.97]	"Affymetrix [400,496]"	N
11/25/2008	18179892	Wallace	10-Jan-08	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia	Serum urate	"1,955 hypertensive individuals"	"2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)"	4p16.1	"SLC2A9,WDR1"	rs7442295-A	rs7442295	0.79	2.00E-15		0.02	[0.02-0.03] mMol/L higher	"Affymetrix [400,496]"	N
11/25/2008	18159244	Hinney	26-Dec-07	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/18159244?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants	Obesity (early onset extreme)	"487 young cases, 442 controls"	"2,269 individuals in 644 families"	16q12.2	FTO	rs1121980-T	rs1121980	0.41	1.00E-07		1.66	[1.37-2.01]	"Affymetrix [440,794]"	N
11/25/2008	18073375	Duggan	19-Dec-07	J Natl Cancer Inst	http://www.ncbi.nlm.nih.gov/pubmed/18073375?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP	Prostate cancer	"1,235 cases, 1,599 controls"	"1,242 cases, 917 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina & Affymetrix [60,275]"	N
11/25/2008	18084291	van Es	16-Dec-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"737 cases, 721 controls"	"1,030 cases, 1,195 controls"	7q36.2	DPP6	rs10260404-C	rs10260404	0.35	5.00E-08		1.3	[1.18-1.43]	"Illumina [311,946]"	N
11/25/2008	18084291	van Es	16-Dec-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"737 cases, 721 controls"	"1,030 cases, 1,195 controls"	15q22.1	LIPC	rs3825776-?	rs3825776	0.29	0.000009		1.34	[1.20-1.46]	"Illumina [311,946]"	N
11/25/2008	18084291	van Es	16-Dec-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"737 cases, 721 controls"	"1,030 cases, 1,195 controls"	2p24.2	Intergenic	rs7580332-?	rs7580332	0.45	0.000009		1.22	[1.09-1.35]	"Illumina [311,946]"	N
11/25/2008	18057069	Cronin	7-Dec-07	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/18057069?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of sporadic ALS in a homogenous Irish population	Amyotrophic lateral sclerosis	"221 cases, 211 controls"	"737 cases, 721 controls"	7q36.2	DPP6	rs10260404-?	rs10260404	0.37	0.000003		1.37	[1.20-1.56]	"Illumina [497,917]"	N
11/25/2008	18075462	Suzuki	17-Nov-07	Pharmacogenet Genomics	http://www.ncbi.nlm.nih.gov/pubmed/18075462?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis	Coronary spasm	"50 Japanese female cases, 50 Japanese female controls"	"151 Japanese female cases, 160 Japanese female controls"	14q21.1	Intergenic	rs10498345-T	rs10498345	0.3	9.00E-07		2.33	[1.64-3.23]	"Affymetrix [97,552]"	N
11/25/2008	17998437	Li	12-Nov-07	Arch Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17998437?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease	Alzheimer's disease	"753 cases, 736 controls"	"418 cases, 249 controls"	19q13.32	"APOE, APOC"	rs4420638-?	rs4420638	NR	2.00E-44		NR	NR	"Affymetrix [469,438]"	N
11/25/2008	17997608	Li	9-Nov-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17997608?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	The GLUT9 Gene Is Associated with Serum Uric Acid Levels in Sardinia and Chianti Cohorts	Serum urate	"4,305 Sardinian individuals"	"1,301 Tuscan individuals"	4p16.1	GLUT9	rs6855911-A	rs6855911	0.74	2.00E-16		0.32	[NR] mg/dl higher	"Affymetrix [362,129]"	N
11/25/2008	17982456	Plenge	4-Nov-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17982456?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two independent alleles at 6q23 associated with risk of rheumatoid arthritis	Rheumatoid arthritis	"397 cases, 1,211 Framingham individuals"	"2,283 cases, 3,258 controls"	6q23.3	"TNFAIP3, OLIG3"	rs10499194-C	rs10499194	0.71	1.00E-09		1.33	[1.15-1.52]	"Affymetrix [79,853]"	N
11/25/2008	17982456	Plenge	4-Nov-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17982456?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Two independent alleles at 6q23 associated with risk of rheumatoid arthritis	Rheumatoid arthritis	"397 cases, 1,211 Framingham individuals"	"2,283 cases, 3,258 controls"	6q23.3	"TNFAIP3, OLIG3"	rs6920220-?	rs6920220	0.2	1.00E-07		1.22	[NR]	"Affymetrix [79,853]"	N
11/25/2008	17975299	Webster	1-Nov-07	Neurodegener Dis	http://www.ncbi.nlm.nih.gov/pubmed/17975299?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sorl1 as an Alzheimer's disease predisposition gene?	Alzheimer's disease	"664 cases, 422 controls"	NR	19q13.32	APOE	rs4420638-?	rs4420638	NR	1.00E-39		NR	NR	"Affymetrix [~502,627]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blond vs. brown hair color	"2,986 individuals"	"3,932 individuals"	14q32.12	SLC24A4	rs12896399-T	rs12896399	0.44	1.00E-48		2.56	[2.12-3.09]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blond vs. brown hair color	"2,986 individuals"	"3,932 individuals"	16q24.3	MC1R	rs1805007-T	rs1805007	0.08	2.00E-13		2.34	[1.69-3.24]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blond vs. brown hair color	"2,986 individuals"	"3,932 individuals"	15q13.1	OCA2	rs1667394-A	rs1667394	0.88	6.00E-35		4.94	[3.16-7.71]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blond vs. brown hair color	"2,986 individuals"	"3,932 individuals"	12q21.33	KITLG	rs12821256-C	rs12821256	0.14	4.00E-30		2.32	[1.86-2.92]	"Illumina [317,511]"	N
2/16/2009	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blue vs. brown eyes	"2,986 individuals"	"3,932 individuals"	15q13.1	OCA2	rs1667394-A	rs1667394	0.88	0		29.43	[21.47-40.35]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blue vs. green eyes	"2,986 individuals"	"3,932 individuals"	11q14.3	TYR	rs1393350-A	rs1393350	0.23	3.00E-12		1.52	[1.28-1.81]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blue vs. green eyes	"2,986 individuals"	"3,932 individuals"	14q32.12	SLC24A4	rs12896399-T	rs12896399	0.4	4.00E-38		2.06	[1.76-2.42]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Blue vs. green eyes	"2,986 individuals"	"3,932 individuals"	15q13.1	OCA2	rs1667394-A	rs1667394	0.98	2.00E-53		6.74	[4.61-9.83]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Freckles	"2,986 individuals"	"3,932 individuals"	11q14.3	TYR	rs1042602-C	rs1042602	0.67	2.00E-11		1.32	[1.17-1.49]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Freckles	"2,986 individuals"	"3,932 individuals"	16q24.3	MC1R	rs1805007-T	rs1805007	0.05	1.00E-96		4.37	[3.56-5.37]	"Illumina [317,511]"	N
11/25/2008	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Freckles	"2,986 individuals"	"3,932 individuals"	6p25.3	"SEC5L1,IRF4"	rs1540771-A	rs1540771	0.42	4.00E-18		1.4	[1.26-1.57]	"Illumina [317,511]"	N
2/16/2009	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Red vs non-red hair color	"2,986 individuals"	"3,932 individuals"	16q24.3	MC1R	rs1805007-T	rs1805007	NR	0		12.47	[9.37-16.60]	"Illumina [317,511]"	N
2/16/2009	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Skin sensitivity to sun	"2,986 individuals"	"3,932 individuals"	11q14.3	TYR	rs1393350-A	rs1393350	0.27	2E-06		1.26	[1.11-1.43]	"Illumina [317,511]"	N
2/16/2009	17952075	Sulem	21-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2	"Genetic determinants of hair, eye and skin pigmentation in Europeans"	Skin sensitivity to sun	"2,986 individuals"	"3,932 individuals"	16q24.3	MC1R	rs1805007-T	rs1805007	0.06	2.00E-55		2.94	[2.42-3.58]	"Illumina [317,511]"	N
11/25/2008	17999355	Stokowski	15-Oct-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genomewide association study of skin pigmentation in a South Asian population	Skin pigmentation	363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution	"116 low maxL*, 115 high maxL* individuals"	15q21.1	SLC24A5	rs1834640-G	rs1834640	0.08	1.00E-50		12.5	[8.33-20.0]	"Perlegen [1,502,205] (pooled)"	N
11/25/2008	17999355	Stokowski	15-Oct-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genomewide association study of skin pigmentation in a South Asian population	Skin pigmentation	363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution	"116 low maxL*, 115 high maxL* individuals"	11q14.3	TYR	rs1042602-C	rs1042602	0.84	4.00E-10		4.36	[2.64-7.20]	"Perlegen [1,502,205] (pooled)"	N
11/25/2008	17999355	Stokowski	15-Oct-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genomewide association study of skin pigmentation in a South Asian population	Skin pigmentation	363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution	"116 low maxL*, 115 high maxL* individuals"	5p13.3	SLC45A2	rs16891982-C	rs16891982	0.83	3.00E-11		4.86	[2.88-8.21]	"Perlegen [1,502,205] (pooled)"	N
11/25/2008	17934461	Broderick	14-Oct-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17934461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk	Colorectal cancer	"940 cases, 965 controls"	"7,473 cases, 5,984 controls"	18q21.1	SMAD7	rs4939827-T	rs4939827	0.52	1.00E-12		1.16	[1.09-1.27]	"Illumina [547,647]"	N
11/25/2008	17911428	Cervino	8-Oct-07	Ann NY Acad Sci	http://www.ncbi.nlm.nih.gov/pubmed/17911428?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide study of lupus: preliminary analysis and data release	Lupus	"51 cases, 114 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [241,701]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1q23.2	"FCER1A,OR10J3"	rs2494250-?	rs2494250	NR	1.00E-14	(MCP1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	14q23.2	Intergenic	rs8005745-?	rs8005745	NR	4E-06	(CD40L)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1q23.2	CRP	rs2794520-?	rs2794520	NR	3.00E-08	"(CRP average 2,6,7)"	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1p31.1	Intergenic	rs7552393-?	rs7552393	NR	5.00E-07	(TNFA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	19q12	ZNF536	rs746961-?	rs746961	NR	8.00E-07	(CRP6)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	4q31.1	"CLGN, ELMOD2"	rs17532515-?	rs17532515	NR	1.00E-06	(Bilirubin)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	9q21.32	Intergenic	rs1998303-?	rs1998303	NR	0.000001	(AAT)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1q23.2	IGSF4B	rs10489849-?	rs10489849	NR	0.000001	(MCP1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	15q21.3	Intergenic	rs10518765-?	rs10518765	NR	1.00E-06	(AlkPhos)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	10q26.2	"PTPRE, MKI67"	rs2387326-?	rs2387326	NR	1.00E-06	(VitKPhylloq)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	5q23.2	Intergenic	rs1119582-?	rs1119582	NR	1.00E-06	"(CRP average 2,6,7)"	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	6q15	Intergenic	rs10485165-?	rs10485165	NR	1.00E-06	(VitD25OH)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	6q21	Intergenic	rs1417352-?	rs1417352	NR	2E-06	(ANP6)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	10q21.1	Intergenic	rs583012-?	rs583012	NR	2E-06	(CRP2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	7p13	Intergenic	rs1486139-?	rs1486139	NR	2E-06	(ANP6)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	13q14.11	Intergenic	rs10492681-?	rs10492681	NR	2E-06	(ALT2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	13q21.1	Intergenic	rs10507577-?	rs10507577	NR	0.000003	(VitD25OH)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	11q23.2	DRD2	rs1079596-?	rs1079596	NR	0.000003	(ANP6)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1q23.2	IGSF4B	rs1474747-?	rs1474747	NR	0.000003	(MCP1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	7p21.3	Intergenic	rs7778619-?	rs7778619	NR	0.000003	(CD40L)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903293	Benjamin	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with select biomarker traits in the Framingham Heart Study	Select biomarker traits	"1,012 individuals (Framingham)"	NR	1q23.2	OR10J1	rs4128725-?	rs4128725	NR	4.00E-12	(MCP1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903300	Fox	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project	Body mass index	"1,341 individuals (Framingham)"	NR	7q32.3	Intergenic	rs1106683-?	rs1106683	NR	1.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903300	Fox	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project	Body mass index	"1,341 individuals (Framingham)"	NR	7q23.3	Intergenic	rs1106684-?	rs1106684	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903300	Fox	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project	Body mass index	"1,341 individuals (Framingham)"	NR	13q21.32	Intergenic	rs1333026-?	rs1333026	NR	8E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903300	Fox	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project	Waist circumference traits	"1,341 individuals (Framingham)"	NR	8q21.1	GDAP1	rs4471028-?	rs4471028	NR	2.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903300	Fox	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project	Waist circumference traits	"1,341 individuals (Framingham)"	NR	3q13.31	Intergenic	rs1875517-?	rs1875517	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903308	Gottlieb	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association of sleep and circadian phenotypes	Sleep duration	738 individuals (Framingham)	NR	3p22.1	MYR1P	rs6599077-?	rs6599077	NR	1.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903308	Gottlieb	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association of sleep and circadian phenotypes	Sleep duration	738 individuals (Framingham)	NR	13q21.2	Intergenic	rs10492604-?	rs10492604	NR	4E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903308	Gottlieb	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association of sleep and circadian phenotypes	Sleepiness	738 individuals (Framingham)	NR	5q11.2	PDE4D	rs1823068-?	rs1823068	NR	3.00E-08	(sleepiness)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903308	Gottlieb	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association of sleep and circadian phenotypes	Sleepiness	738 individuals (Framingham)	NR	8q13.3	EYA1	rs2218488-?	rs2218488	NR	0.000003	(sleepiness)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Cystatin C	"810-1,010 individuals depending on measure (Framingham)"	NR	20p11.21	"CST9L, CST9, CST3"	rs1158167-?	rs1158167	NR	9.00E-09		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Thyroid stimulating hormone	"810-1,010 individuals depending on measure (Framingham)"	NR	7p15.3	Intergenic	rs6977660-?	rs6977660	NR	4E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Thyroid stimulating hormone	"810-1,010 individuals depending on measure (Framingham)"	NR	6q21	HACE1	rs9322817-?	rs9322817	NR	7E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Thyroid stimulating hormone	"810-1,010 individuals depending on measure (Framingham)"	NR	7p15.3	RAPGEF5	rs10499559-?	rs10499559	NR	8E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Urinary albumin excretion	"810-1,010 individuals depending on measure (Framingham"	NR	11q23.2	FAM55B	rs1712790-?	rs1712790	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903292	Hwang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study	Urinary albumin excretion	"810-1,010 individuals depending on measure (Framingham"	NR	21q21.3	Intergenic	rs9305354-?	rs9305354	NR	8E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903299	Kathiresan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903299?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study	Blood lipid traits	"1,087 individuals (Framingham)"	"~8,100 individuals"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	13q21.31	Intergenic	rs9317284-?	rs9317284	NR	2.00E-07	(FNBMDm)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	4p16.1	Intergenic	rs9291683-?	rs9291683	NR	2E-06	(BUA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	20q11.23	CTNNBL1	rs4811196-?	rs4811196	NR	1.00E-06	(TRBMDf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	16q23.3	Intergenic	rs4087296-?	rs4087296	NR	3.00E-07	(TRBMDf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	12q21.1	Intergenic	rs10506701-?	rs10506701	NR	1.00E-06	(TRBMD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	10p15.2	Intergenic	rs2165468-?	rs2165468	NR	1.00E-06	(FNBMDm)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	7q35	CNTNAP2	rs2214681-?	rs2214681	NR	0.000003	(BUA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Bone mineral density	"1,141 individuals (Framingham)"	NR	3p24.1	RBMS3	rs10510628-?	rs10510628	NR	0.000003	(TRBMDm)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	5q13.2	ZNF366	rs10515148-?	rs10515148	NR	6.00E-07	(NeckZ1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	12q21.31	Intergenic	rs10506821-?	rs10506821	NR	2.00E-07	(ShaftW1f)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	5q14.3	GPR98	rs10514345-?	rs10514345	NR	2.00E-07	(NeckZ1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	11q14.1	Intergenic	rs1452928-?	rs1452928	NR	7.00E-07	(ShaftW1f)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	12p13.31	VAMP1	rs10492096-?	rs10492096	NR	0.000003	(ShaftZ1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	13q13.3	Intergenic	rs1590305-?	rs1590305	NR	0.000003	(NeckZ1rm)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	18q12.1	Intergenic	rs4131805-?	rs4131805	NR	2E-06	(NSAm)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	3q12.3	Intergenic	rs991258-?	rs991258	NR	5.00E-07	(ShaftW1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	3p14.1	Intergenic	rs922948-?	rs922948	NR	2E-06	(ShaftW1f)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	1p11.2	Intergenic	rs6600671-?	rs6600671	NR	6.00E-07	(NeckZ1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	3p24.3	KCNH8	rs2053506-?	rs2053506	NR	4E-06	(NeckZ1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	6p24.1	PHACTR1	rs4715166-?	rs4715166	NR	0.000003	(NeckW1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	3p14.3	ERC2	rs2054989-?	rs2054989	NR	6.00E-07	(NeckW1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	5p14.1	Intergenic	rs2548003-?	rs2548003	NR	2.00E-07	(NeckZ1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	8p12	NRG1	rs10503887-?	rs10503887	NR	2.00E-07	(ShaftZ1R)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903296	Kiel	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with bone mass and geometry in the Framingham Heart Study	Hip geometry	"1,141 individuals (Framingham)"	NR	11q23.2	Intergenic	rs638882-?	rs638882	NR	4E-06	(NeckZ1rf)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903304	Larson	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes	Atrial fibrillation	"1,341-1,345 individuals, depending on measure (Framingham)"	NR	11q22.1	CNTN5	rs10501920-?	rs10501920	NR	0.000009		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903304	Larson	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes	Atrial fibrillation	"1,341-1,345 individuals, depending on measure (Framingham)"	NR	15q23	Intergenic	rs4776472-?	rs4776472	NR	0.000008		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903304	Larson	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes	Atrial fibrillation	"1,341-1,345 individuals, depending on measure (Framingham)"	NR	13q14	Intergenic	rs958546-?	rs958546	NR	0.000005		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903304	Larson	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes	Heart failure	"1,341-1,345 individuals, depending on measure (Framingham"	NR	10q25.3	KIAA1598	rs740363-?	rs740363	NR	0.000009		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903304	Larson	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes	Major CVD	"1,341-1,345 individuals, depending on measure (Framingham)"	NR	6p24.1	Intergenic	rs499818-?	rs499818	NR	7E-06	(major CVD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	14q24.3	Intergenic	rs935334-?	rs935334	NR	0.000003	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	8q13.3	Intergenic	rs1963982-?	rs1963982	NR	0.000003	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	1p31.3	Intergenic	rs10493340-?	rs10493340	NR	2E-06	(SBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	2q36.3	"CCL20, WDR69"	rs7591163-?	rs7591163	NR	3.00E-07	(DBPLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	16q23.3	CDH13	rs3096277-?	rs3096277	NR	1.00E-09	(SBPLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	6q15	Intergenic	rs2509458-?	rs2509458	NR	7E-06	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	14q24.3	C14orf118	rs2121070-?	rs2121070	NR	0.000005	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	5q22.1	CAMK4	rs10491334-?	rs10491334	NR	4E-06	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Blood pressure	"644-1,327 individuals, depending on measure (Framingham)"	NR	3p26.3	CNTN4	rs4370013-?	rs4370013	NR	4E-06	(DBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	6q25.2	SYNE1	rs1322512-?	rs1322512	NR	8E-06	(MAP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	5q14.3	MEF2C	rs770189-?	rs770189	NR	0.000003	(CB-PWV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	7q33	EXOC4	rs10488172-?	rs10488172	NR	8E-06	(RWLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	3q24	SLC9A9	rs1371924-?	rs1371924	NR	4E-06	(RWLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	1q25.1	TNR	rs3766680-?	rs3766680	NR	4E-06	(FWLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	17p12	HS3ST3A1	rs10521232-?	rs10521232	NR	4E-06	(CF-PWVLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	2q14.3	CNTNAP5	rs1367248-?	rs1367248	NR	0.000003	(CF-PWVLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	13q13.3	GPC6	rs6492654-?	rs6492654	NR	2E-06	(RWLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	8p22	VPS37A	rs3793427-?	rs3793427	NR	2E-06	(FWLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	3p24.1	TGFBR2	rs3773643-?	rs3773643	NR	2.00E-07	(MAPLTA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	20q13.13	PREX1	rs6063312-?	rs6063312	NR	2E-06	(RW)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	9q31.2	Intergenic	rs7042864-?	rs7042864	NR	0.000006	(CB-PWV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903302	Levy	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness	Tonometry	"644-1,327 individuals, depending on measure (Framingham"	NR	3p22.3	Intergenic	rs10514688-?	rs10514688	NR	0.000006	(CB-PWV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	12p11.22	Intergenic	rs1463605-?	rs1463605	NR	7.00E-08	(biologic age)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	7q21.11	Intergenic	rs2371208-?	rs2371208	NR	0.000003	(age at death)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	2p12	Intergenic	rs10496262-?	rs10496262	NR	3.00E-07	(age at natural menopause)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	2q24.1	GALNT13	rs958672-?	rs958672	NR	2E-06	(age at natural menopause)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	1q42.3	GNG4	rs291353-?	rs291353	NR	0.000006	(age at natural menopause)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	11q14.3	Intergenic	rs1528753-?	rs1528753	NR	8.00E-08	(age at death)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	2p12	Intergenic	rs10496265-?	rs10496265	NR	1.00E-08	(age at natural menopause)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	3q25.31	KCNAB1	rs3772255-?	rs3772255	NR	8E-06	(biologic age)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	15q25.3	KLHL25	rs7176093-?	rs7176093	NR	7E-06	(biologic age)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study	Aging traits	"1,345 individuals (Framingham)"	NR	12q24.23	CCDC60	rs7137869-?	rs7137869	NR	6.00E-07	(walking speed exam 7)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	"1,345 individuals (Framingham)"	NR	16q21	Intergenic	rs2639889-?	rs2639889	NR	9.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	"1,345 individuals (Framingham)"	NR	6p24.3	Intergenic	rs10484246-?	rs10484246	NR	8.00E-08		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	"1,345 individuals (Framingham)"	NR	5p15.32	Intergenic	rs32566-?	rs32566	NR	2.00E-09		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	"1,345 individuals (Framingham)"	NR	8p22	Intergenic	rs4831837-?	rs4831837	NR	5.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903295	Lunetta	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Morbidity-free survival	"1,345 individuals (Framingham)"	NR	1q24.2	DPT	rs1412337-?	rs1412337	NR	2.00E-09		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Diabetes (incident)	"1,087 individuals (Framingham)"	NR	2q32.3	TMEFF2	rs10497721-?	rs10497721	NR	7.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Diabetes related insulin traits	"1,087 individuals (Framingham)"	NR	7p15.1	CPVL	rs10486607-?	rs10486607	NR	8E-06	(HbA1C)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Diabetes related insulin traits	"1,087 individuals (Framingham)"	NR	13q21.33	Intergenic	rs2066219-?	rs2066219	NR	0.000009	(ISI_0-120)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Diabetes related insulin traits	"1,087 individuals (Framingham)"	NR	14q12	Intergenic	rs2877832-?	rs2877832	NR	2E-06	(FI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Diabetes related insulin traits	"1,087 individuals (Framingham)"	NR	14q12	Intergenic	rs2877832-?	rs2877832	NR	0.000003	(HOMA-IR)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	3p24.1	Intergenic	rs10510634-?	rs10510634	NR	0.000005	(tFPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	8p11.21	ZMAT4	rs2722425-?	rs2722425	NR	2.00E-08	(tFPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	4q27	PRDM5	rs180730-?	rs180730	NR	0.000005	(FPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	8p11.21	ZMAT4	rs2722425-?	rs2722425	NR	0.000009	(FPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	5q23.3	Intergenic	rs7731657-?	rs7731657	NR	7E-06	(tFPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903298	Meigs	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association with diabetes-related traits in the Framingham Heart Study	Fasting plasma glucose	"1,087 individuals (Framingham)"	NR	4q27	PRDM5	rs180730-?	rs180730	NR	0.000006	(tFPG)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	13q32.1	ABCC4	rs1926657-?	rs1926657	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	7q11.22	Intergenic	rs10263639-?	rs10263639	NR	0.000003		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	12q21.1	Intergenic	rs1154865-?	rs1154865	NR	7.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	18q21.2	Intergenic	rs1978503-?	rs1978503	NR	1.00E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	5q34	Intergenic	rs6556756-?	rs6556756	NR	5.00E-07		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	15q21.1	FBN1	rs1876206-?	rs1876206	NR	0.000006		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	17q21.33	COL1A1	rs2075555-?	rs2075555	NR	8.00E-08		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	2p16.1	Intergenic	rs10490113-?	rs10490113	NR	0.000005		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Breast cancer	"1,345 individuals (Framingham)"	NR	21q21.3	GRIK1	rs458685-?	rs458685	NR	0.000006		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Prostate cancer	"1,345 individuals (Framingham)"	NR	3q24	Intergenic	rs345013-?	rs345013	NR	0.000005		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Prostate cancer	"1,345 individuals (Framingham)"	NR	5q14.3	HAPLN1	rs4466137-?	rs4466137	NR	0.000003		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Prostate cancer	"1,345 individuals (Framingham)"	NR	6p12.2	PKHD1	rs10498792-?	rs10498792	NR	0.000003		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Prostate cancer	"1,345 individuals (Framingham)"	NR	13q33.1	Intergenic	rs1529276-?	rs1529276	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903305	Murabito	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study	Prostate cancer	"1,345 individuals (Framingham)"	NR	3p22.2	CTDSPL	rs9311171-?	rs9311171	NR	2E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903306	Newton-Cheh	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study	Electrocardiographic traits	"548-1,175 individuals, depending on measure (Framingham)"	NR	13q12.2	RPL21	rs10507380-?	rs10507380	NR	8E-06	(QT interval)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903306	Newton-Cheh	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study	Electrocardiographic traits	"548-1,175 individuals, depending on measure (Framingham)"	NR	2q22.1	Intergenic	rs882300-?	rs882300	NR	3.00E-07	(PR interval)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903306	Newton-Cheh	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study	Heart rate variability traits	"548-1,175 individuals, depending on measure (Framingham)"	NR	4q34	NEIL3	rs1395479-?	rs1395479	NR	7E-06	(LF/HF)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903306	Newton-Cheh	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study	Heart rate variability traits	"548-1,175 individuals, depending on measure (Framingham)"	NR	13q13.3	DCAMKL1	rs9315385-?	rs9315385	NR	8E-06	(TP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Coronary artery calcification	"673-984 individuals, depending on measure (Framingham)"	NR	1p22.2	Intergenic	rs2390582-?	rs2390582	NR	1.00E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Coronary artery calcification	"673-984 individuals, depending on measure (Framingham)"	NR	14q24.2	NUMB	rs10483853-?	rs10483853	NR	0.000006		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Coronary artery calcification	"673-984 individuals, depending on measure (Framingham)"	NR	12q23.2	DR1M	rs10507130-?	rs10507130	NR	7E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	5p15.2	DNAH5	rs2896103-?	rs2896103	NR	0.000005	(ABI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	11q14.3	Intergenic	rs1350445-?	rs1350445	NR	0.000009	(ABI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	4q28.1	Intergenic	rs1320267-?	rs1320267	NR	7E-06	(ABI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	1q31.1	Intergenic	rs1400544-?	rs1400544	NR	0.000006	(CCA IMT)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	5p15.2	DNAH5	rs1502050-?	rs1502050	NR	0.000009	(ABI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	10q11.22	LRRC18	rs3849150-?	rs3849150	NR	2E-06	(AAC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	2q33.2	ABI2	rs1376877-?	rs1376877	NR	4.00E-07	(ICA IMT)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903303	O'Donnell	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study	Subclinical atherosclerosis traits (other)	"673-984 individuals, depending on measure (Framingham)"	NR	5p15.2	DNAH5	rs7715811-?	rs7715811	NR	0.000006	(ABI)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	12p11.1	Intergenic	rs9300212-?	rs9300212	NR	8E-06	(WRAT)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	9q22.2	DIRAS2	rs1831521-?	rs1831521	NR	8E-06	(Nam)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	2q22.1	Intergenic	rs934299-?	rs934299	NR	0.000009	(F3)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	1p22.2	Intergenic	rs2179965-?	rs2179965	NR	1.00E-06	(F3)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	4q13.2	Intergenic	rs1155865-?	rs1155865	NR	2E-06	(Nam)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	21q21.3	Intergenic	rs2832077-?	rs2832077	NR	2E-06	(F3)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	6p23	Intergenic	rs6914079-?	rs6914079	NR	2E-06	(F2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	1q42.2	TARBP1	rs10489896-?	rs10489896	NR	0.000006	(F2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	11q25	NCAPD3	rs1031381-?	rs1031381	NR	0.000006	(F3)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	17q22	PPM1E	rs9303401-?	rs9303401	NR	0.000005	(NAM)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	11q14.1	Intergenic	rs530965-?	rs530965	NR	4E-06	(Nam)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	12q23.3	"POLR3B, RFX4"	rs3891355-?	rs3891355	NR	0.000003	(Sim)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	5q32	Intergenic	rs9325032-?	rs9325032	NR	0.000003	(F2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Cognitive test performance	705 individuals (Framingham)	NR	14q24.3	Intergenic	rs2352904-?	rs2352904	NR	2E-06	(F2)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Volumetric brain MRI	705 individuals (Framingham)	NR	4q31.3	Intergenic	rs360929-?	rs360929	NR	0.000009	(ALTHBV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Volumetric brain MRI	705 individuals (Framingham)	NR	20q13.33	CDH4	rs1970546-?	rs1970546	NR	4.00E-08	(ATCBV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Volumetric brain MRI	705 individuals (Framingham)	NR	11q23.2	NNMT	rs2847476-?	rs2847476	NR	0.000003	(ALLV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Volumetric brain MRI	705 individuals (Framingham)	NR	11p13	EHF	rs5028798-?	rs5028798	NR	0.000003	(ATBV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903297	Seshadri	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study	Volumetric brain MRI	705 individuals (Framingham)	NR	11q22.1	CNTN5	rs952700-?	rs952700	NR	0.000006	(AFBV)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	4p15.31	SLIT2	rs1379659-?	rs1379659	NR	1.00E-07	(LVDD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	1p31.3	PDE4B	rs10493389-?	rs10493389	NR	7E-06	(LAD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	2q36.1	Intergenic	rs10498091-?	rs10498091	NR	0.000006	(LVM)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	1q31.1	FAM5C	rs1935881-?	rs1935881	NR	0.000006	(LAD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	8q13.3	KCNB2	rs10504543-?	rs10504543	NR	0.000005	(LVSD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	4p15.31	SLIT2	rs666088-?	rs666088	NR	0.000005	(LVDD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	6q15	SPACA1	rs366676-?	rs366676	NR	2E-06	(LVFS)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Echocardiographic traits	"1,238 individuals (Framingham)"	NR	5q14.3	Intergenic	rs4920799-?	rs4920799	NR	7E-06	(LVDD)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Endothelial function traits	"1,238 individuals (Framingham)"	NR	10q24.33	OBFC1	rs3814219-?	rs3814219	NR	9.00E-07	(BABF)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Exercise treadmill test traits	"1,238 individuals (Framingham)"	NR	11q22.3	Intergenic	rs746463-?	rs746463	NR	0.000005	(P3MRSBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Exercise treadmill test traits	"1,238 individuals (Framingham)"	NR	8p12	WRN	rs2553268-?	rs2553268	NR	0.000006	(S2ESBP)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Exercise treadmill test traits	"1,238 individuals (Framingham)"	NR	4q25	NOLA1	rs6847149-?	rs6847149	NR	0.000003	(S2EHR)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903301	Vasan	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study"	Exercise treadmill test traits	"1,238 individuals (Framingham)"	NR	1q43	RYR2	rs2819770-?	rs2819770	NR	4E-06	(S2EHR)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Mean forced vital capacity from 2 exams	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	4q25	Intergenic	rs10516541-?	rs10516541	NR	4E-06	(meanfvc)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Mean forced vital capacity from 2 exams	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	7q21.3	COL1A2	rs441051-?	rs441051	NR	2E-06	(meanfvc)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	15q26.1	FLJ32831	rs1455782-?	rs1455782	NR	4E-06	(ppfvc)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	15q11.2	SNRPN	rs3867498-?	rs3867498	NR	1.00E-06	(fev1slope)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	21q22.3	ADARB1	rs2838815-?	rs2838815	NR	0.000003	(meanratio)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	7q34	Intergenic	rs357394-?	rs357394	NR	0.000009	(ppfvc)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	17p12	CDRT4	rs2906966-?	rs2906966	NR	8E-06	(ppfev1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	1q21.3	IL6R	rs4129267-?	rs4129267	NR	7E-06	(ppfef)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	14q23.1	Intergenic	rs808225-?	rs808225	NR	7E-06	(ppfefrat)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	14q22.1	NID2	rs730532-?	rs730532	NR	0.000006	(ppfef)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	2q36.3	RHBDD1	rs3820928-?	rs3820928	NR	0.000005	(ppfev1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903307	Wilk	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Framingham Heart Study genome-wide association: results for pulmonary function measures	Pulmonary function traits (other)	"1,097-1,222 individuals, depending on measure (Framingham)"	NR	8q11.22	SNTG1	rs310558-?	rs310558	NR	0.000005	(ppratio)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Factor VII	"1,000 individuals (Framingham)"	NR	7p22.2	Intergenic	rs10488360-?	rs10488360	0.3	7E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Factor VII	"1,000 individuals (Framingham)"	NR	1p36.32	Intergenic	rs966321-?	rs966321	0.47	8E-06		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Factor VII	"1,000 individuals (Framingham)"	NR	13q34	"MCF2L, AB116074, AK092739, AK123267, AB0023600, F7, CR603372, F10, PROZ"	rs561241-?	rs561241	0.12	5.00E-16		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Factor VII	"1,000 individuals (Framingham)"	NR	3p26.1	Intergenic	rs4591494-?	rs4591494	0.19	0.000009		NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	6q25.1	MAP3K7IP2	rs727979-?	rs727979	0.14	8E-06	(RBCC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	20p12.3	Intergenic	rs6108011-?	rs6108011	0.28	0.000006	(RBCC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	14q21.3	MAMDC1	rs7159841-?	rs7159841	0.21	2.00E-07	(Viscosity)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	1q23.2	"OR10J1,OR10J5"	rs4133289-?	rs4133289	0.19	2.00E-07	(Hgb)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	5q21.3	Intergenic	rs4460176-?	rs4460176	0.29	0.000003	(PAI-1)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	1p31.1	NEGR1	rs10493485-?	rs10493485	0.29	2E-06	(tPA)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	11q24.1	Intergenic	rs565229-?	rs565229	0.1	4E-06	(pltcoll)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	14q32.2	Intergenic	rs10484128-?	rs10484128	0.15	0.000006	(pltadp)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	11q11	"OR5AP2, OR5AR1, OR9G1, OR9G4"	rs1397048-?	rs1397048	0.4	7.00E-08	(MCH)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	10p11.21	ANKRD30A	rs1200821-?	rs1200821	0.47	0.000006	(MCH)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	5q21.1	Intergenic	rs1829883-?	rs1829883	0.41	0.000006	(MCH)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	8q24.13	Intergenic	rs7844723-?	rs7844723	0.45	2E-06	(Hgb)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	2p16.2	Intergenic	rs2357013-?	rs2357013	0.45	0.000006	(Hgb)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	6q25.1	Intergenic	rs636864-?	rs636864	0.21	0.000006	(RBCC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	4p15.33	Intergenic	rs10489087-?	rs10489087	0.13	0.000005	(RBCC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	2p16.2	Intergenic	rs1160297-?	rs1160297	0.43	1.00E-06	(Hgb)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	12q14.2	Intergenic	rs10506458-?	rs10506458	0.13	0.000005	(pltcoll)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17903294	Yang	19-Sep-07	BMC Med Genet	http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study	Hemostatic factors and hematological phenotypes	"1,000 individuals (Framingham"	NR	1p34.3	"FLJ11730, BC016328"	rs9253-?	rs9253	0.18	4E-06	(RBCC)	NR	NR	"Affymetrix [70,897]"	N
11/25/2008	17848626	Florez	10-Sep-07	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/17848626?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets	Type 2 diabetes and 6 quantitative traits	"1,087 family members"	"1,465 unrelated individuals; 2,175 cases and 2,412 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [66,543]"	N
11/25/2008	17846125	Hanson	10-Sep-07	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/17846125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array	Type 2 diabetes	"300 cases, 334 controls, 121 nondiabetic siblings, 140 diabetic siblings"	"1,207 cases, 1,627 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [80,044]"	N
11/25/2008	17846124	Hayes	10-Sep-07	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/17846124?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies	Type 2 diabetes	"281 cases, 280 controls"	"~1,979 cases, ~3,092 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [88,142]"	N
11/25/2008	17846126	Rampersaud	10-Sep-07	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/17846126?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations	Type 2 diabetes	"124 cases, 295 controls"	"2,142 cases, 2,117 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [82,485]"	N
11/25/2008	17827064	van Es	7-Sep-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17827064?ordinalpos=13&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study	Amyotrophic lateral sclerosis	"737 cases, 721 controls"	"1,030 cases, 1,195 controls"	12p11	ITPR2	rs2306677-?	rs2306677	0.07	0.000003		1.58	[1.30-1.91]	"Illumina [311,946]"	N
11/25/2008	17804836	Plenge	5-Sep-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study	Rheumatoid arthritis	"1,493 cases, 1,831 controls"	"1,053 cases, 1,858 controls"	1p13.2	PTPN22	rs2476601-?	rs2476601	0.1	2.00E-11		1.72	[NR]	"Illumina [297,086]"	N
11/25/2008	17804836	Plenge	5-Sep-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study	Rheumatoid arthritis	"1,493 cases, 1,831 controls"	"1,053 cases, 1,858 controls"	9q34	TRAF1-C5	rs3761847-G	rs3761847	0.41	4.00E-14		1.32	[1.23-1.42]	"Illumina [297,086]"	N
11/25/2008	17804836	Plenge	5-Sep-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study	Rheumatoid arthritis	"1,493 cases, 1,831 controls"	"1,053 cases, 1,858 controls"	6p21.32	HLA-DRB1	rs660895-?	rs660895	0.21	1.00E-108		3.62	[NR]	"Illumina [297,086]"	N
11/25/2008	17804789	Raelson	5-Sep-07	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci	Crohn's disease	382 trios	"750 cases, 828 controls, 521 trios"	16q12.1	NOD2	rs5743289-?	rs5743289	NR	6.00E-17		NR	NR	"Perlegen [164,279]"	N
11/25/2008	17804789	Raelson	5-Sep-07	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci	Crohn's disease	382 trios	"750 cases, 828 controls, 521 trios"	1p31.3	IL23R	17 marker haplotype-1	"rs11465802,rs2064689,rs2902440,rs1343151,rs10889676,rs9988642,rs12567232,rs6669582,rs10789230,rs11209026,rs11465804,rs11209003,rs11209002,rs1004819,rs2201841,rs10889677"	0.23	1.00E-08		1.38	[1.23-1.53]	"Perlegen [164,279]"	N
11/25/2008	17804789	Raelson	5-Sep-07	Proc Natl Acad Sci USA	http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci	Crohn's disease	382 trios	"750 cases, 828 controls, 521 trios"	1p31.3	IL23R	17 marker haplotype-2	"rs11209002,rs2064689,rs1004819,rs2902440,rs11465802,rs2201841,rs11465804,rs11209026,rs1343151,rs10889676,rs10889677,rs9988642,rs12567232,rs6669582,rs10789230,rs11209003"	0.97	2.00E-07		2.56	[1.75-3.70]	"Perlegen [164,279]"	N
11/25/2008	17767159	Menzel	2-Sep-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15	F-cell distribution	179 adults in upper and lower 5%	90 adults	2p15.1	BCL11A	rs1427407-?	rs1427407	0.14	6.00E-31		13.1	[NR] % of variance explained	"Illumina [308,015]"	N
11/25/2008	17767159	Menzel	2-Sep-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15	F-cell distribution	179 adults in upper and lower 5%	90 adults	6q23.3	Intergenic	rs9399137-?	rs9399137	0.23	3.00E-36		15.8	[NR] % of variance explained	"Illumina [308,015]"	N
11/25/2008	17767159	Menzel	2-Sep-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15	F-cell distribution	179 adults in upper and lower 5%	90 adults	11p15.5	HBB	NR	NR	0.33	2.00E-38		10.2	[NR] % of variance explained	"Illumina [308,015]"	N
11/25/2008	17767157	Weedon	2-Sep-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17767157?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common variant of HMGA2 is associated with adult and childhood height in the general population	Height	"4,921 individuals"	"29,098 individuals (19,064 adults)"	12q14.3	HMGA2	rs1042725-C	rs1042725	0.51	6.00E-16		0.4	[NR] cm per copy in adult height	"Affymetrix [364,301]"	N
11/25/2008	17690259	Thorleifsson	9-Aug-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17690259?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma	Glaucoma (exfoliation)	"75 cases, 14,474 controls"	"254 cases, 198 controls"	15q24.1	LOXL1	rs3825942-G	rs3825942	0.85	3.00E-21		20.1	[10.80-37.41]	"Illumina [304,250]"	N
11/25/2008	17684544	Franke	8-Aug-07	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Systematic association mapping identifies NELL1 as a novel IBD disease gene	Crohn's disease	"393 cases, 399 controls"	"1,248 trios, 2,920 cases, 1,961 controls"	5p13.1	PTGER4	rs1992660-?	rs1992660	0.39	4.00E-07		1.42	[1.24-1.67]	"Affymetrix [92,387]"	N
11/25/2008	17684544	Franke	8-Aug-07	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Systematic association mapping identifies NELL1 as a novel IBD disease gene	Crohn's disease	"393 cases, 399 controls"	"1,248 trios, 2,920 cases, 1,961 controls"	11p15.1	NELL1	rs1793004-?	rs1793004	0.27	0.000003		1.3	[1.12-1.52]	"Affymetrix [92,387]"	N
11/25/2008	17684544	Franke	8-Aug-07	PLoS ONE	http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Systematic association mapping identifies NELL1 as a novel IBD disease gene	Crohn's disease	"393 cases, 399 controls"	"1,248 trios, 2,920 cases, 1,961 controls"	16q12.1	CARD15	rs2076756-?	rs2076756	0.27	1.00E-21		1.71	[1.42-2.05]	"Affymetrix [92,387]"	N
11/25/2008	17671248	Dunckley	1-Aug-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17671248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Whole-genome analysis of sporadic amyotrophic lateral sclerosis	Amyotrophic lateral sclerosis	"386 cases, 542 controls"	"901 cases, 1,025 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix and Illumina [776,955]"	N
11/25/2008	17653210	Maeda	1-Aug-07	Kidney Int Suppl	http://www.ncbi.nlm.nih.gov/pubmed/17653210?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population	Diabetic nephropathy	"94 cases, 94 controls"	NR	7p14.2	ELMO1	rs741301-?	rs741301	NR	8E-06		2.67	[1.71-4.16]	"NR [~80,000]"	N
11/25/2008	17667963	Shifman	31-Jul-07	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/17667963?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A whole genome association study of neuroticism using DNA pooling	Neuroticism	"1,038 cases, 1,016 controls"	"831 cases, 702 controls"	5q11.2	PDE4D	rs702543-A	rs702543	0.55	2E-06		1.27	[1.15-1.40]	"Affymetrix [452,574] (pooled)"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	6p21.32	HLA-DRA	rs3135388-A	rs3135388	0.23	9.00E-81		1.99	[1.84-2.15]	"Affymetrix [334,923]"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	10p15.1	IL2RA	rs12722489-C	rs12722489	0.85	3.00E-08		1.25	[1.11-1.36]	"Affymetrix [334,923]"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	5p13.2	IL7RA	rs6897932-C	rs6897932	0.75	3.00E-07		1.18	[1.11-1.26]	"Affymetrix [334,923]"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	16p13	KIAA0350	rs6498169-G	rs6498169	0.37	4E-06		1.14	[1.08-1.21]	"Affymetrix [334,923]"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	1p22	RPL5	rs6604026-C	rs6604026	0.29	8E-06		1.15	[1.08-1.22]	"Affymetrix [334,923]"	N
11/25/2008	17660530	Hafler	29-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Risk alleles for multiple sclerosis identified by a genomewide study	Multiple sclerosis	"931 trios, 2,431 controls"	"609 trios, 2,322 cases, 2,987 controls"	9q33	DBC1	rs10984447-A	rs10984447	0.77	8E-06		1.17	[1.09-1.25]	"Affymetrix [334,923]"	N
11/25/2008	17611496	Moffatt	26-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17611496?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma	Asthma	"994 cases, 1,243 controls"	"2,320 cases, 3,301 controls"	17q12	ORMDL3	rs7216389-T	rs7216389	0.52	9.00E-11		1.45	[1.17-1.81]	"Illumina [307,328]"	N
11/25/2008	17658951	Scuteri	20-Jul-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits	Obesity-related traits	"4,741 individuals"	"3,205 individuals"	16q12.2	FTO	rs9930506-A	rs9930506	0.54	9.00E-07	(BMI)	0.13	[NR] SD lower (BMI)	"Affymetrix [362,129]"	N
11/25/2008	17658951	Scuteri	20-Jul-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits	Obesity-related traits	"4,741 individuals"	"3,205 individuals"	16q12.2	FTO	rs9930506-A	rs9930506	0.54	3.00E-08	(hip)	0.16	[NR] SD lower (hip)	"Affymetrix [362,129]"	N
11/25/2008	17658951	Scuteri	20-Jul-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits	Obesity-related traits	"4,741 individuals"	"3,205 individuals"	16q12.2	FTO	rs9930506-A	rs9930506	0.54	9.00E-07	(weight)	0.12	[NR] SD lower (weight)	"Affymetrix [362,129]"	N
11/25/2008	17641165	Fellay	19-Jul-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17641165?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A whole-genome association study of major determinants for host control of HIV-1	HIV1 viral setpoint	486 patients	140 patients	NR	NR	NR		NR	NS	NS	NR	NR	"Illumina [535,101]"	N
11/25/2008	17634447	Stefansson	19-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634447?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genetic risk factor for periodic limb movements in sleep	Restless legs syndrome	"306 cases, 15,664 controls"	"311 cases, 1,895 controls"	6p21.2	BTBD9	rs3923809-A	rs3923809	0.66	1.00E-17		1.9	[1.50-2.20]	"Illumina [306,937]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	9p21.3	Intergenic	rs1333049-C	rs1333049	0.47	3.00E-19		1.36	[1.27-1.46]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	1q41	MIA3	rs17465637-C	rs17465637	0.29	1.00E-06		1.2	[1.12-1.30]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	15q22.33	SMAD3	rs17228212-C	rs17228212	0.3	2.00E-07		1.21	[1.13-1.30]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	1p13.3	PSRC1	rs599839-A	rs599839	0.23	4.00E-09		1.29	[1.18-1.40]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	10q11.21	CXCL12	rs501120-T	rs501120	0.13	9.00E-08		1.33	[1.20-1.48]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	2q36.3	pseudogene	rs2943634-C	rs2943634	0.65	2.00E-07		1.21	[1.13-1.30]	"Affymetrix [377,857]"	N
11/25/2008	17634449	Samani	18-Jul-07	N Engl J Med	http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genomewide association analysis of coronary artery disease	Coronary disease	"1,926 cases, 2,938 controls"	"875 cases, 1,644 controls"	6q25.1	MTHFD1L	rs6922269-A	rs6922269	0.25	3.00E-08		1.23	[1.15-1.33]	"Affymetrix [377,857]"	N
11/25/2008	17637780	Winkelmann	18-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions	Restless legs syndrome	"401 cases, 1,644 controls"	"1,158 cases, 1,178 controls"	15q23	"MAP2K5, LBXCOR1"	rs12593813-G	rs12593813	0.67	1.00E-15		1.5	[1.36-1.66]	"Affymetrix [236,758]"	N
11/25/2008	17637780	Winkelmann	18-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions	Restless legs syndrome	"401 cases, 1,644 controls"	"1,158 cases, 1,178 controls"	2p14	MEIS1	rs2300478-G	rs2300478	0.24	3.00E-28		1.74	[1.57-1.92]	"Affymetrix [236,758]"	N
11/25/2008	17637780	Winkelmann	18-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions	Restless legs syndrome	"401 cases, 1,644 controls"	"1,158 cases, 1,178 controls"	6p21.2	BTBD9	rs9296249-T	rs9296249	0.76	4.00E-18		1.67	[1.49-1.89]	"Affymetrix [236,758]"	N
11/25/2008	17632509	Buch	15-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17632509?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease	Gallstones	"280 cases, 360 controls"	"2,000 cases, 1,202 controls"	2p21	ABCG8	rs11887534-C	rs11887534	0.1	1.00E-14		2.2	[1.80-2.60]	"Affymetrix [382,492]"	N
11/25/2008	17632545	Hakonarson	15-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene	Type 1 diabetes	"467 trios, 561 cases, 1,143 controls"	"2,350 individuals in 549 families; 390 trios"	16p13.13	KIAA0350	rs2903692-G	rs2903692	0.62	7.00E-11		1.54	[1.32-1.79]	"Illumina [543,071]"	N
11/25/2008	17632545	Hakonarson	15-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene	Type 1 diabetes	"467 trios, 561 cases, 1,143 controls"	"2,350 individuals in 549 families; 390 trios"	1p13.2	PTPN22	rs2476601-A	rs2476601	0.09	1.00E-07		1.8	[1.44-2.24]	"Illumina [543,071]"	N
11/25/2008	17632545	Hakonarson	15-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene	Type 1 diabetes	"467 trios, 561 cases, 1,143 controls"	"2,350 individuals in 549 families; 390 trios"	6p21.32	HLA-E	rs2647044-A	rs2647044	0.13	1.00E-16		8.3	[6.97-9.89]	"Illumina [543,071]"	N
11/25/2008	17632545	Hakonarson	15-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene	Type 1 diabetes	"467 trios, 561 cases, 1,143 controls"	"2,350 individuals in 549 families; 390 trios"	11p15.5	INS	rs1004446-C	rs1004446	0.65	4.00E-09		1.61	[1.37-1.89]	"Illumina [543,071]"	N
11/25/2008	17618284	Tomlinson	8-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17618284?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21	Colorectal cancer	"930 cases, 960 controls"	"7,334 cases, 5,246 controls"	8q24.21	Intergenic	rs6983267-G	rs6983267	0.49	1.00E-14		1.27	[1.16-1.39]	"Illumina [547,647]"	N
11/25/2008	17618283	Zanke	8-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17618283?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24	Colorectal cancer	"1,257 cases, 1,336 controls"	"6,223 cases, 6,443 controls"	8q24.21	ORF DQ515897	rs10505477-A	rs10505477	0.5	3.00E-11		1.17	[1.12-1.23]	"Illumina and Affymetrix [99,632]"	N
11/25/2008	17603472	Gudbjartsson	1-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17603472?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Variants conferring risk of atrial fibrillation on chromosome 4q25	Atrial fibrillation/atrial flutter	"550 cases, 4,476 controls"	"3,363 cases, 17,616 controls"	4q25	"PITX2,ENPEP"	rs2200733-T	rs2200733	0.11	3.00E-41		1.72	[1.59-1.86]	"Illumina [316,515]"	N
11/25/2008	17603472	Gudbjartsson	1-Jul-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17603472?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Variants conferring risk of atrial fibrillation on chromosome 4q25	Atrial fibrillation/atrial flutter	"550 cases, 4,476 controls"	"3,363 cases, 17,616 controls"	4q25	"PITX2,ENPEP"	rs10033464-T	rs10033464	0.08	7.00E-11		1.39	[1.26-1.53]	"Illumina [316,515]"	N
11/25/2008	17603485	Gudmundsson	1-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17603485?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes"	Prostate cancer	"1,501 cases, 11,290 controls"	"1,992 cases, 3,058 controls"	17q12	TCF2	rs4430796-A	rs4430796	0.49	1.00E-11		1.22	[1.15-1.30]	"Illumina [310,520]"	N
11/25/2008	17603485	Gudmundsson	1-Jul-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17603485?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes"	Prostate cancer	"1,501 cases, 11,290 controls"	"1,992 cases, 3,058 controls"	17q24.3	Intergenic	rs1859962-G	rs1859962	0.46	3.00E-10		1.2	[1.14-1.27]	"Illumina [310,520]"	N
11/25/2008	17668382	Salonen	26-Jun-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17668382?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium	Type 2 diabetes	"500 cases, 497 controls"	"2,573 cases, 2,776 controls"	10q25.2	TCF7L2	rs7903146-A	rs7903146	NR	5.00E-08		1.71	[1.41-2.08]	"Illumina [315,917]"	N
11/25/2008	17668382	Salonen	26-Jun-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17668382?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium	Type 2 diabetes	"500 cases, 497 controls"	"2,573 cases, 2,776 controls"	2q12.1	Intergenic	rs6712932-?	rs6712932	NR	0.000006		1.52	[1.27-1.82]	"Illumina [315,917]"	N
11/25/2008	17558408	van Heel	10-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17558408?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21	Celiac disease	"778 cases, 1,422 controls"	"991 cases, 1,489 controls"	6p21.32	HLA-DQA1	rs2187668-A	rs2187668	0.14	1.00E-19		7.04	[6.08-8.15]	"Illumina [310,605]"	N
11/25/2008	17558408	van Heel	10-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17558408?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21	Celiac disease	"778 cases, 1,422 controls"	"991 cases, 1,489 controls"	4q27	"KIAA1109,TENR,IL2,IL21"	rs6822844-G	rs6822844	0.82	1.00E-14		1.59	[1.41-1.75]	"Illumina [310,605]"	N
11/25/2008	17553421	Reiman	7-Jun-07	Neuron	http://www.ncbi.nlm.nih.gov/pubmed/17553421?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers	Alzheimer's disease (late onset)	"446 cases, 290 controls"	"415 cases, 260 controls"	11q14.1	GAB2	rs2373115-G	rs2373115	0.7	1.00E-10		4.06	[2.81-14.69]	"Affymetrix [312,316]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	16p12.1	"PALB2,NDUFAB1,DCTN5"	rs420259-A	rs420259	0.72	6.00E-08		2.08	[1.60-2.71]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	3q27	NR	rs683395-G	rs683395	0.08	0.000005		1.47	[1.26-1.71]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	6p21	NR	rs6458307-?	rs6458307	0.69	4E-06		1.19	[1.04-1.33]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	2q37	NR	rs2953145-C	rs2953145	0.23	7E-06		1.84	[1.31-2.58]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	14q23.1	NR	rs10134944-T	rs10134944	0.09	7E-06		1.45	[1.24-1.68]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	20p13	NR	rs3761218-C	rs3761218	0.64	7E-06		1.03	[1.15-1.23]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Bipolar disorder	"1,868 cases, 2,938 controls"	NR	14q32.33	NR	rs11622475-C	rs11622475	0.3	8E-06		1.13	[0.89-1.44]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Coronary disease	"1,926 cases, 2,938 controls"	(see Samani 2007)	22q12	NR	rs688034-T	rs688034	0.31	4E-06		1.11	[0.99-1.25]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Coronary disease	"1,926 cases, 2,938 controls"	(see Samani 2007)	16q23	NR	rs8055236-G	rs8055236	0.2	0.000006		1.91	[1.33-2.74]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Coronary disease	"1,926 cases, 2,938 controls"	(see Samani 2007)	1q43	NR	rs17672135-C	rs17672135	0.87	2E-06		1.43	[1.23-1.64]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Coronary disease	"1,926 cases, 2,938 controls"	(see Samani 2007)	9p21.3	"CDKN2A,CDKN2B"	rs1333049-C	rs1333049	0.47	1.00E-13		1.47	[1.27-1.70]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	2q37.1	ATG16L1	rs10210302-T	rs10210302	0.48	5.00E-14		1.19	[1.01-1.41]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	5p13.1	Intergenic	rs17234657-G	rs17234657	0.13	2.00E-12		1.54	[1.34-1.76]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	10q21.2	Intergenic	rs10761659-G	rs10761659	0.46	2E-06		1.23	[1.05-1.45]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	5q31.1	Intergenic	rs6596075-C	rs6596075	0.17	0.000003		1.55	[1.00-2.39]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	6p21	NR	rs9469220-A	rs9469220	0.48	2E-06		1.14	[0.98-1.32]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	1p31.3	IL23R	rs11805303-T	rs11805303	0.68	6.00E-12		1.39	[1.22-1.58]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	16q12.1	NOD2	rs17221417-G	rs17221417	0.29	4.00E-11		1.29	[1.13-1.46]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	10q24.2	NKX2-3	rs10883365-G	rs10883365	0.48	6.00E-08		1.2	[1.03-1.39]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	7q36.1	NR	rs7807268-G	rs7807268	0.46	4E-06		1.38	[1.20-1.60]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	10p15.1	NR	rs6601764-C	rs6601764	0.41	0.000009		1.16	[1.01-1.33]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	5q33.1	IRGM	rs1000113-T	rs1000113	0.07	3.00E-07		1.54	[1.31-1.82]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	18p11.21	PTPN2	rs2542151-G	rs2542151	0.16	2.00E-07		1.3	[1.14-1.48]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Crohn's disease	"1,748 cases, 2,938 controls"	(see Parkes 2007)	3p21.31	"BSN, MST1"	rs9858542-A	rs9858542	0.28	4.00E-08		1.09	[0.96-1.24]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Hypertension	"1,952 cases, 2,938 controls"	NR	15q26	NR	rs2398162-A	rs2398162	0.26	0.000006		1.31	[1.03-1.67]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Hypertension	"1,952 cases, 2,938 controls"	NR	1q43	"RYR2,CHRM3,ZP4"	rs2820037-T	rs2820037	0.14	8.00E-07		1.54	[1.03-2.31]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	6p21.32	MHC	rs6457617-T	rs6457617	0.49	5.00E-75		2.36	[1.97-2.84]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	1p13.2	PTPN22	rs6679677-A	rs6679677	0.1	6.00E-25		1.98	[1.72-2.27]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	6p21.32	HLA-DRB1	rs615672-?	rs615672	NR	8.00E-27		NR	NR	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	7q32.3	Intergenic	rs11761231-C	rs11761231	0.62	4.00E-07	(sex-differentiated)	1.32	[NR] (women)	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	22q13	NR	rs743777-G	rs743777	0.29	1.00E-06		1.09	[0.97-1.24]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	4p15.2	NR	rs3816587-C	rs3816587	0.41	0.000009		1.09	[0.96-1.25]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Rheumatoid arthritis	"1,860 cases, 2,938 controls"	NR	21q22	NR	rs2837960-G	rs2837960	0.17	2E-06		1.05	[0.93-1.20]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	6p21.32	MHC	rs9272346-G	rs9272346	0.61	0		5.49	[4.83-6.24]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	1p13.2	PTPN22	rs6679677-A	rs6679677	0.1	5.00E-26		1.82	[1.59-2.09]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	5q31.1	NR	rs17166496-G	rs17166496	0.61	0.000005		1.3	[1.15-1.47]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	12p13.31	NR	rs3764021-C	rs3764021	0.47	5.00E-08		1.57	[1.38-1.79]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	4q27	NR	rs17388568-A	rs17388568	0.26	0.000003		1.26	[1.11-1.42]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	12q13.2	ERBB3	rs11171739-C	rs11171739	0.42	1.00E-11		1.34	[1.17-1.54]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	12q24.13	"SH2B3,LNK,TRAFD1,PTPN1"	rs17696736-G	rs17696736	0.42	2.00E-14		1.34	[1.16-1.53]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	16p13.13	KIAA0350	rs12708716-A	rs12708716	0.65	5.00E-07		1.19	[0.97-1.45]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	12p13	NR	rs11052552-G	rs11052552	0.49	7.00E-07		1.49	[1.28-1.73]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 1 diabetes	"1,963 cases, 2,938 controls"	(see Todd 2007)	4q27	NR	rs6534347-A	rs6534347	0.35	2E-06		1.3	[1.10-1.55]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	10q25.2	TCF7L2	rs4506565-T	rs4506565	0.32	5.00E-12		1.36	[1.20-1.54]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	4q27	NR	rs7659604-T	rs7659604	0.38	0.000009		1.35	[1.19-1.54]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	12q13	NR	rs12304921-G	rs12304921	0.15	7E-06		2.5	[1.53-4.09]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	12q15	NR	rs1495377-G	rs1495377	0.5	7E-06		1.28	[1.11-1.49]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	3p14	NR	rs358806-?	rs358806	0.8	0.000003		1.16	[1.03-1.33]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	6p22.3	CDKAL1	rs9465871-C	rs9465871	0.18	3.00E-07		1.18	[1.04-1.34]	"Affymetrix [469,557]"	N
11/25/2008	17554300	WTCCC	7-Jun-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls"	Type 2 diabetes	"1,924 cases, 2,938 controls"	(see Zeggini 2007)	16q12.2	FTO	rs9939609-A	rs9939609	0.4	2.00E-07		1.34	[1.17-1.52]	"Affymetrix [469,557]"	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	10q24.2	NKX2-3	rs10883365-?	rs10883365	0.48	4.00E-10		1.18	[1.05-1.32]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	5q33.1	IRGM	rs13361189-?	rs13361189	0.08	2.00E-10		1.38	[1.15-1.66]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	3p21.31	MST1	rs9858542-?	rs9858542	0.29	5.00E-08		1.17	[1.14-1.31]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	1q31.2	Intergenic	rs10801047-?	rs10801047	0.08	3.00E-08		1.47	[1.22-1.76]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	18p11.21	PTPN2	rs2542151-?	rs2542151	0.18	3.00E-08		1.15	[1.00-1.32]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	1q24.3	Intergenic	rs12035082-?	rs12035082	0.4	2.00E-07		1.14	[1.02-1.27]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	5q33.3	IL12B	rs6887695-?	rs6887695	0.32	0.000009		1.26	[1.12-1.41]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	5p13.1	Intergenic	rs9292777-?	rs9292777	0.4	3.00E-18		1.34	[1.20-1.50]	see WTCCC	N
11/25/2008	17554261	Parkes	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility	Crohn's disease	"1,748 cases, 2,938 controls"	"1,182 cases, 2,024 controls"	21q22.2	Intergenic	rs2836754-?	rs2836754	0.35	5.00E-07		1.15	[1.03-1.28]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	18p11.21	PTPN2	rs2542151-C	rs2542151	0.16	1.00E-14		1.3	[1.22-1.40]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	18q22.2	CD226	rs763361-A	rs763361	0.47	1.00E-08		1.16	[1.10-1.22]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	1p13.2	PTPN22	rs2476601-T	rs2476601	0.09	2.00E-80		1.98	[1.82-2.15]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	2q24.2	IFIH1	rs1990760-A	rs1990760	0.6	2.00E-11		1.18	[1.11-1.23]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	5p13.2	CAPSL	rs1445898-G	rs1445898	0.55	8E-06		1.12	[1.06-1.19]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	5p13.2	IL7R	rs6897932-G	rs6897932	0.71	8E-06		1.12	[1.06-1.19]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	2p11.2	"AFF3, LOC150577"	rs9653442-G	rs9653442	0.46	0.000005		1.11	[1.05-1.17]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	1p13.2	"PHTF1, PTPN22"	rs6679677-A	rs6679677	0.1	8.00E-24		1.89	[1.67-2.13]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	11p15.5	INS	rs3741208-T	rs3741208	0.38	2.00E-07		1.25	[1.15-1.35]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	12q24.13	C12orf30	rs17696736-G	rs17696736	0.42	2.00E-16		1.22	[1.15-1.28]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	12q13.2	ERBB3	rs2292239-A	rs2292239	0.34	2.00E-20		1.28	[1.21-1.35]	see WTCCC	N
11/25/2008	17554260	Todd	6-Jun-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes	Type 1 diabetes	"1,963 cases, 2,938 controls"	"2997 trios, 4,000 cases, 5,000 controls"	16p13.13	KIAA0350	rs12708716-A	rs12708716	0.68	3.00E-18		1.23	[1.16-1.30]	see WTCCC	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	10q26.13	FGFR2	rs2981582-G	rs2981582	0.38	2.00E-76		1.26	[1.23-1.30]	"Perlegen [205,586]"	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	5q11.2	MAP3K1	rs889312-A	rs889312	0.28	7.00E-20		1.13	[1.10-1.16]	"Perlegen [205,586]"	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	5p12	Intergenic	rs981782-C	rs981782	0.53	0.000009		1.04	[1.01-1.08]	"Perlegen [205,586]"	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	8q24.21	Intergenic	rs13281615-T	rs13281615	0.4	5.00E-12		1.08	[1.05-1.11]	"Perlegen [205,586]"	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	11p15.5	LSP1	rs3817198-T	rs3817198	0.3	3.00E-09		1.07	[1.04-1.11]	"Perlegen [205,586]"	N
11/25/2008	17529967	Easton	27-May-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies novel breast cancer susceptibility loci	Breast cancer	"390 cases, 364 controls"	"26,646 cases, 24,889 controls"	16q12.1	"TNCR9,LOC643714"	rs3803662-C	rs3803662	0.25	1.00E-36		1.2	[1.16-1.24]	"Perlegen [205,586]"	N
11/25/2008	17529973	Hunter	27-May-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17529973?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer	Breast cancer	"1,145 cases, 1,142 controls"	"1,176 cases, 2,072 controls"	10q26.13	FGFR2	rs1219648-G	rs1219648	0.4	1.00E-10		1.2	[1.07-1.42]	"Illumina [528,173]"	N
11/25/2008	17529974	Stacey	27-May-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17529974?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer	Breast cancer	"1,599 cases, 11,546 controls"	"2,934 cases, 5,967 controls"	2q35	Intergenic	rs13387042-A	rs13387042	0.5	1.00E-13		1.2	[1.14-1.26]	"Illumina [311,524]"	N
11/25/2008	17529974	Stacey	27-May-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17529974?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer	Breast cancer	"1,599 cases, 11,546 controls"	"2,934 cases, 5,967 controls"	16q12.1	TNRC9	rs3803662-T	rs3803662	0.27	6.00E-19		1.28	[1.21-1.35]	"Illumina [311,524]"	N
11/25/2008	17505501	Kindmark	15-May-07	Pharmacogenomics J	http://www.ncbi.nlm.nih.gov/pubmed/17505501?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis	Response to ximelagatran treatment	"74 cases, 130 controls"	"10 cases, 16 controls"	6p21.3	HLA-DRB1	DRB1*07		NR	0.000009		4.41	[2.20-8.87]	"Perlegen [~266,722]"	N
11/25/2008	17486107	Baum	8-May-07	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/17486107?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder	Bipolar disorder	"461 cases, 563 controls"	"772 cases, 876 controls"	13q14.11	DGKH	rs1012053-A	rs1012053	0.84	2.00E-08		1.59	[1.35-1.87]	"Illumina [555,235] (pooled)"	N
11/25/2008	17434096	Matarin	6-May-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release	Stroke	"259 cases, 269 controls"	NR	18p11.2	IMPA2	rs7506045-?	rs7506045	0.1	7.00E-07		5.39	[2.77-10.5]	"Illumina [408,803]"	N
11/25/2008	17434096	Matarin	6-May-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release	Stroke	"259 cases, 269 controls"	NR	7p21	Intergenic	rs10486776-?	rs10486776	0.1	0.000006		5.62	[2.66-11.9]	"Illumina [408,803]"	N
11/25/2008	17434096	Matarin	6-May-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release	Stroke	"259 cases, 269 controls"	NR	6q21	AIM1	rs783396-?	rs783396	0.9	0.000009		2.17	[1.47-3.13]	"Illumina [408,803]"	N
11/25/2008	17434096	Matarin	6-May-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release	Stroke	"259 cases, 269 controls"	NR	13q21.1	Intergenic	rs9536591-?	rs9536591	0.1	0.000006		1.92	[1.41-2.63]	"Illumina [408,803]"	N
11/25/2008	17478679	Helgadottir	3-May-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17478679?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common variant on chromosome 9p21 affects the risk of myocardial infarction	Myocardial infarction	"1,607 cases, 6,728 controls"	"2,980 cases, 6,309 controls"	9p21.3	"CDKN2A,CDKN2B"	rs10757278-G	rs10757278	0.45	1.00E-20		1.28	[1.22-1.35]	"Illumina [305,953]"	N
11/25/2008	17478681	McPherson	3-May-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17478681?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common allele on chromosome 9 associated with coronary heart disease	Coronary disease	"322 cases, 312 controls"	"3,984 cases, 19,807 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Perlegen [72,864]"	N
11/25/2008	17470457	Huentelman	30-Apr-07	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/17470457?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance	Episodic memory	341 young adults	472 young adults	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~502,627] (pooled)"	N
2/13/2009	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Triglycerides	"up to 5,217 individuals"	NR	19q13.32	APOE cluster	rs4420638-G	rs4420638	0.22	3.00E-13	(LDL)	2.4	% [NR] of variance explained	"Affymetrix [386,731]"	N
2/13/2009	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Triglycerides	"up to 5,217 individuals"	NR	2p24.1	APOB	rs693-A	rs693	0.49	7.00E-07	(LDL)	NR	NR	"Affymetrix [386,731]"	N
2/13/2009	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Triglycerides	"up to 5,217 individuals"	NR	16q13	CETP	rs1800775-C	rs1800775	0.47	3.00E-13	(HDL)	2.1	% [NR] of variance explained	"Affymetrix [386,731]"	N
2/13/2009	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Triglycerides	"up to 5,217 individuals"	NR	8p21.3	LPL	rs328-T	rs328	0.1	5.00E-07	(TG)	1	% [NR] of variance explained	"Affymetrix [386,731]"	N
2/13/2009	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Triglycerides	"up to 5,217 individuals"	NR	16q13	CETP	rs1800775-C	rs1800775	0.44	0.000003	(apoA-1)	1.6	% [NR] of variance explained	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.65	5.00E-08	(DGI+FUSION+WTCCC)	1.12	[1.07-1.16]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3p25.2	PPARG	rs1801282-C	rs1801282	0.86	0.000002	(DGI+FUSION+WTCCC)	1.14	[1.08-1.20]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q23.33	HHEX	rs1111875-C	rs1111875	0.53	6.00E-10	(DGI+FUSION+WTCCC)	1.13	[1.08-1.17]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	6p22.3	CDKAL1	rs7754840-C	rs7754840	0.31	4.00E-11	(DGI+FUSION+WTCCC)	1.12	[1.08-1.16]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q25.2	TCF7L2	rs7903146-T	rs7903146	0.26	2.00E-31		1.38	[1.31-1.46]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3q27.2	IGF2BP2	rs4402960-T	rs4402960	0.29	2.00E-09		1.17	[1.11-1.23]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	9p21.3	"CDKN2A,CDKN2B"	rs10811661-T	rs10811661	0.83	5.00E-08		1.2	[1.12-1.28]	"Affymetrix [386,731]"	N
11/25/2008	17463246	Saxena	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels	Type 2 diabetes	"1,464 cases, 1,467 controls"	"5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	11p15.1	KCNJ11	rs5219-T	rs5219	0.47	1.00E-07		1.15	[1.09-1.21]	"Affymetrix [386,731]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3q27.2	IGF2BP2	rs4402960-T	rs4402960	0.3	9.00E-16	(DGI+FUSION+WTCCC)	1.14	[1.11-1.18]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	6p22.3	CDKAL1	rs7754840-C	rs7754840	0.36	4.00E-11	(DGI+FUSION+WTCCC)	1.12	[1.08-1.16]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	9p21.3	"CDKN2A,CDKN2B"	rs10811661-T	rs10811661	0.85	8.00E-15	(DGI+FUSION+WTCCC)	1.2	[1.14-1.25]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	11p12	Intergenic	rs9300039-C	rs9300039	0.89	6.00E-08		1.48	[1.28-1.71]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	16q12.2	FTO	rs8050136-A	rs8050136	0.38	1.00E-12	(DGI+FUSION+WTCCC)	1.17	[1.12-1.22]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	11p15.1	KCNJ11	rs5219-T	rs5219	0.46	7.00E-11	(DGI+FUSION+WTCCC)	1.14	[1.10-1.19]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q23.33	HHEX	rs1111875-C	rs1111875	0.52	6.00E-10	(DGI+FUSION+WTCCC)	1.13	[1.09-1.17]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.61	5.00E-08	(DGI+FUSION+WTCCC)	1.12	[1.07-1.16]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3p25.2	PPARG	rs1801282-C	rs1801282	0.82	0.000002	(DGI+FUSION+WTCCC)	1.14	[1.08-1.20]	"Illumina [315,635]"	N
11/25/2008	17463248	Scott	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants	Type 2 diabetes	"1,161 cases, 1,174 controls"	"1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q25.2	TCF7L2	rs7903146-T	rs7903146	0.18	1.00E-08		1.34	[1.21-1.49]	"Illumina [315,635]"	N
11/25/2008	17460697	Steinthorsdottir	26-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes	Type 2 diabetes	"1,399 EA cases, 5,275 EA controls"	"2,437 EA cases, 7,287 EA controls"	10q25.2	TCF7L2	rs7903146-?	rs7903146	0.3	2.00E-10		1.38	[NR]	"Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]"	N
11/25/2008	17460697	Steinthorsdottir	26-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes	Type 2 diabetes	"1,399 EA cases, 5,275 EA controls"	"2,437 EA cases, 7,287 EA controls"	6p22.3	CDKAL1	rs7756992-G	rs7756992	0.26	8.00E-09		1.2	[1.13-1.27]	"Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]"	N
11/25/2008	17460697	Steinthorsdottir	26-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A variant in CDKAL1 influences insulin response and risk of type 2 diabetes	Type 2 diabetes	"1,399 EA cases, 5,275 EA controls"	"2,437 EA cases, 7,287 EA controls"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.67	0.000003		1.15	[1.08-1.22]	"Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	16q12.2	FTO	rs8050136-A	rs8050136	0.4	7.00E-14		1.23	[1.18-1.32]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3p25.2	PPARG	rs1801282-C	rs1801282	NR	0.000002	(DGI+FUSION+WTCCC)	1.14	[1.08-1.20]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	9p21.3	"CDKN2A, CDKN2B"	rs564398-T	rs564398	0.56	0.000001		1.13	[1.08-1.19]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	9p21.3	"CDKN2A, CDKN2B"	rs10811661-T	rs10811661	0.83	0.000005		1.19	[1.11-1.28]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q25.2	TCF7L2	rs7901695-C	rs7901695	NR	1.00E-48	(DGI+FUSION+WTCCC)	1.37	[1.31-1.43]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	10q23.33	HHEX	rs5015480-C	rs5015480	0.57	0.000005		1.13	[1.07-1.19]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	6p22.3	CDKAL1	rs10946398-C	rs10946398	0.32	1.00E-08		1.16	[1.10-1.22]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	3q27.2	IGF2BP2	rs4402960-T	rs4402960	0.32	9.00E-16	(DGI+FUSION+WTCCC)	1.14	[1.11-1.18]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.69	5.00E-08	(DGI+FUSION+WTCCC)	1.12	[1.07-1.16]	"Affymetrix [393,453]"	N
11/25/2008	17463249	Zeggini	26-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes	Type 2 diabetes	"1,924 cases, 2,938 controls"	"3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)"	11p15.1	KCNJ11	rs5215-C	rs5215	NR	5.00E-11	(DGI+FUSION+WTCCC)	1.14	[1.10-1.19]	"Affymetrix [393,453]"	N
11/25/2008	17435756	Rioux	15-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis	Crohn's disease	"946 cases, 977 controls"	"530 trios, 353 cases, 207 controls"	1p31.3	IL23R	rs7517847-?	rs7517847	0.4	3.00E-12		NR	NR	"Illumina [304,413]"	N
11/25/2008	17435756	Rioux	15-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis	Crohn's disease	"946 cases, 977 controls"	"530 trios, 353 cases, 207 controls"	2q37.1	ATG16L1	rs2241880-G	rs2241880	0.55	1.00E-13		1.45	[1.27-1.64]	"Illumina [304,413]"	N
11/25/2008	17435756	Rioux	15-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis	Crohn's disease	"946 cases, 977 controls"	"530 trios, 353 cases, 207 controls"	10q21.2	Intergenic	rs224136-?	rs224136	0.81	1.00E-10		1.67	[NR]	"Illumina [304,413]"	N
11/25/2008	17435756	Rioux	15-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis	Crohn's disease	"946 cases, 977 controls"	"530 trios, 353 cases, 207 controls"	16q12.1	CARD15	rs2076756-?	rs2076756	0.24	7.00E-14		NR	NR	"Illumina [304,413]"	N
11/25/2008	17434869	Frayling	12-Apr-07	Science	http://www.ncbi.nlm.nih.gov/pubmed/17434869?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity	Body mass index	"10,657 adults"	"19,424 adults, 10,172 children"	16q12.2	FTO	rs9939609-A	rs9939609	0.39	2.00E-20		0.36	[NR] kg/m2 per copy in adults	"Affymetrix [490,032]"	N
11/25/2008	17407593	Uhl	3-Apr-07	BMC Genetics	http://www.ncbi.nlm.nih.gov/pubmed/17407593?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs"	Nicotine dependence	"134 cases, 320 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~520,000] (pooled)"	N
11/25/2008	17474819	Coon	1-Apr-07	J Clin Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/17474819?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease	Alzheimer's disease (late onset)	"664 cases, 422 controls"	NR	19q13.32	APOE	rs4420638-?	rs4420638	NR	1.00E-39		4.01	[NR]	"Affymetrix [~502,627]"	N
11/25/2008	17401366	Gudmundsson	1-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24	Prostate cancer	"1,453 cases, 3,064 controls"	"1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls"	8q24.21	Intergenic	rs1447295-A	rs1447295	0.09	6.00E-18		1.6	[1.43-1.77]	"Illumina [316,515]"	N
11/25/2008	17401366	Gudmundsson	1-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24	Prostate cancer	"1,453 cases, 3,064 controls"	"1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls"	8q24.21	Intergenic	HapC		0.02 (EA)	3.00E-15	(EA)	2.1	[1.75-2.53] (EA)	"Illumina [316,515]"	N
11/25/2008	17401366	Gudmundsson	1-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24	Prostate cancer	"1,453 cases, 3,064 controls"	"1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls"	8q24.21	Intergenic	rs16901979-A	rs16901979	0.03 (EA)	1.00E-12	(EA)	1.79	[1.53-2.11] (EA)	"Illumina [316,515]"	N
11/25/2008	17395743	Hanson	1-Apr-07	Diabetes	http://www.ncbi.nlm.nih.gov/pubmed/17395743?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study	End-stage renal disease	"105 cases, 102 controls"	NR	8q24.21	PVT1	rs2648875-A	rs2648875	0.53	2E-06		2.97	[1.90-4.65]	"Affymetrix [115,352]"	N
11/25/2008	17401363	Yeager	1-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17401363?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of prostate cancer identifies a second risk locus at 8q24	Prostate cancer	"1,172 cases, 1,157 controls"	"3,124 cases, 3,142 controls"	8q24.21	Intergenic	rs6983267-G	rs6983267	0.5	9.00E-13		1.26	[1.13-1.41]	"Illumina [538,548]"	N
11/25/2008	17401363	Yeager	1-Apr-07	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/17401363?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide association study of prostate cancer identifies a second risk locus at 8q24	Prostate cancer	"1,172 cases, 1,157 controls"	"3,124 cases, 3,142 controls"	8q24.21	Intergenic	rs1447295-A	rs1447295	0.11	2.00E-14		1.43	[1.29-1.59]	"Illumina [538,548]"	N
11/25/2008	17522711	Lencz	20-Mar-07	Mol Psychiatry	http://www.ncbi.nlm.nih.gov/pubmed/17522711?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia	Schizophrenia	"178 cases, 144 controls"	NR	"Xp22.33,Yp11.32"	"CSF2RA,IL3RA"	rs4129148-C	rs4129148	NR	4.00E-07		3.23	[2.04-5.15]	"Affymetrix [439,511]"	N
11/25/2008	17357082	Melquist	8-Mar-07	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/17357082?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms"	Progressive supranuclear palsy	"288 cases, 344 controls"	"213 cases, 391 controls"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [428,867]"	N
11/25/2008	17447842	Libioulle	5-Mar-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4	Crohn's disease	"547 cases, 928 controls"	"1,266 cases, 559 controls, 428 trios"	1p31.3	IL23R	rs11209026-?	rs11209026	0.92	2.00E-18		2.92	[NR]	"Illumina [302,451]"	N
11/25/2008	17447842	Libioulle	5-Mar-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4	Crohn's disease	"547 cases, 928 controls"	"1,266 cases, 559 controls, 428 trios"	5p13.1	Intergenic	rs1373692-?	rs1373692	0.59	2.00E-12		1.46	[NR]	"Illumina [302,451]"	N
11/25/2008	17447842	Libioulle	5-Mar-07	PLoS Genet	http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4	Crohn's disease	"547 cases, 928 controls"	"1,266 cases, 559 controls, 428 trios"	16q12.1	CARD15	rs5743289-?	rs5743289	NR	1.00E-06		NR	NR	"Illumina [302,451]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	10q26.13	Intergenic	rs4363506-?	rs4363506	NR	7.00E-07		1.9	[1.50-2.40]	"Illumina [549,062]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	2p24	Intergenic	rs16984239-?	rs16984239	NR	2E-06		2.1	[1.50-3.00]	"Illumina [549,062]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	8q24.2	Intergenic	rs12680546-?	rs12680546	NR	0.000003		1.67	[1.25-2.00]	"Illumina [549,062]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	20q13.2	ZFP64	rs6013382-?	rs6013382	NR	0.000005		1.43	[1.11-1.67]	"Illumina [549,062]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	4q31.3	KlAA1727	rs11099864-?	rs11099864	NR	0.000009		1	[0.80-1.40]	"Illumina [549,062]"	N
11/25/2008	17362836	Schymick	20-Feb-07	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data	Amyotrophic lateral sclerosis	"276 cases, 276 controls"	NR	9q31.3	SUSD1	rs2782931-?	rs2782931	NR	0.000006		1.11	[0.91-1.43]	"Illumina [549,062]"	N
11/25/2008	17293876	Sladek	11-Feb-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies novel risk loci for type 2 diabetes	Type 2 diabetes	"661 cases, 614 controls"	"2,617 cases, 2,894 controls"	8q24.11	SLC30A8	rs13266634-C	rs13266634	0.7	6.00E-08		1.18	[0.69-1.67]	"Illumina [392,935]"	N
11/25/2008	17293876	Sladek	11-Feb-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies novel risk loci for type 2 diabetes	Type 2 diabetes	"661 cases, 614 controls"	"2,617 cases, 2,894 controls"	10q25.3	TCF7L2	rs7903146-T	rs7903146	0.3	2.00E-34		1.65	"[1.28, 2.02]"	"Illumina [392,935]"	N
11/25/2008	17293876	Sladek	11-Feb-07	Nature	http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies novel risk loci for type 2 diabetes	Type 2 diabetes	"661 cases, 614 controls"	"2,617 cases, 2,894 controls"	10q23.33	HHEX	rs1111875-G	rs1111875	0.6	0.000003		1.19	[0.82-1.56]	"Illumina [392,935]"	N
11/25/2008	17223258	Spinola	16-Jan-07	Cancer Lett	http://www.ncbi.nlm.nih.gov/pubmed/17223258?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide single nucleotide polymorphism analysis of lung cancer risk detects the KLF6 gene	Lung cancer	"338 Italian lung adenocarcinoma cases, 335 Italian controls"	265 Norwegian non-small lung carcinoma cases 356 Norwegian controls	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [~116,204] (pooled)"	N
11/25/2008	17158188	Bierut	7-Dec-06	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/17158188?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Novel genes identified in a high-density genome wide association study for nicotine dependence	Nicotine dependence	"1,050 cases, 879 controls"	NR	21q22.2	NR	rs2836823-T	rs2836823	0.4	2E-06		1.46	[1.23-1.73]	Perlegen [2.4 million] (pooled)	N
11/25/2008	17158188	Bierut	7-Dec-06	Hum Mol Genet	http://www.ncbi.nlm.nih.gov/pubmed/17158188?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Novel genes identified in a high-density genome wide association study for nicotine dependence	Nicotine dependence	"1,050 cases, 879 controls"	NR	10q21.3	CTNNA3	rs4142041-G	rs4142041	0.34	0.000006		1.14	[0.97-1.35]	Perlegen [2.4 million] (pooled)	N
11/25/2008	17099884	Liu	5-Dec-06	Am J Med Genet B Neuropsychiatr Genet	http://www.ncbi.nlm.nih.gov/pubmed/17099884?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	"Addiction molecular genetics: 639,401 SNP whole genome association identifies many ""cell adhesion"" genes"	Addiction	"980 cases, 680 controls"	NR	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [639,401]"	N
11/25/2008	17068223	Duerr	26-Oct-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene	Inflammatory bowel disease	"547 cases, 548 controls"	"401 cases, 433 controls, 883 families, 1,119 affected offspring"	1p31.3	IL23R	rs11209026-A	rs11209026	0.93	4.00E-11		3.84	[2.33-6.66]	"Illumina [308,332]"	N
11/25/2008	17068223	Duerr	26-Oct-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene	Inflammatory bowel disease	"547 cases, 548 controls"	"401 cases, 433 controls, 883 families, 1,119 affected offspring"	1p31.3	IL23R	rs7517847-C	rs7517847	0.56	4.00E-13		1.61	[1.35-1.92]	"Illumina [308,332]"	N
11/25/2008	17068223	Duerr	26-Oct-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene	Inflammatory bowel disease	"547 cases, 548 controls"	"401 cases, 433 controls, 883 families, 1,119 affected offspring"	16q12.1	CARD15	rs2076756-?	rs2076756	NR	5.00E-10		NR	NR	"Illumina [308,332]"	N
11/25/2008	17053149	Papassotiropoulos	20-Oct-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/17053149?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Common Kibra alleles are associated with human memory performance	Memory performance	341 individuals	680 individuals	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [178,390]"	N
11/25/2008	17053108	DeWan	19-Oct-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/17053108?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	HTRA1 promoter polymorphism in wet age-related macular degeneration	Age-related macular degeneration (wet)	"96 Southeast Asian cases, 130 Southeast Asian controls"	NR	10q26	HTRA1	rs11200638-A	rs11200638	NR	8.00E-12		1.6	[0.71-3.61]	"Affymetrix [97,824]"	N
11/25/2008	17052657	Fung	28-Sep-06	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data	Parkinson's disease	"267 cases, 270 controls"	NR	10q11.21	Intergenic	rs1480597-?	rs1480597	NR	2E-06		2.5	[1.67-3.33]	"Illumina [408,803]"	N
11/25/2008	17052657	Fung	28-Sep-06	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data	Parkinson's disease	"267 cases, 270 controls"	NR	4q13.2	BRDG1	rs2242330-?	rs2242330	NR	2E-06		2	[1.43-2.50]	"Illumina [408,803]"	N
11/25/2008	17052657	Fung	28-Sep-06	Lancet Neurol	http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data	Parkinson's disease	"267 cases, 270 controls"	NR	11q14	DLG2	rs10501570-?	rs10501570	NR	7E-06		5	[2.00-12.50]	"Illumina [408,803]"	N
11/25/2008	16648850	Arking	30-Apr-06	Nat Genet	http://www.ncbi.nlm.nih.gov/pubmed/16648850?ordinalpos=10&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization	QT interval prolongation	"100 > 445ms, 100 < 386ms"	"200 > 85th pct, 200 < 15th pct, 7,817 cohort members"	1q23.3	NOS1AP	rs10494366-?	rs10494366	0.36	1.00E-10		4.9	- 7.90 [NR] msec difference between homozygotes	"Affymetrix [88,500]"	N
11/25/2008	16614226	Herbert	14-Apr-06	Science	http://www.ncbi.nlm.nih.gov/pubmed/16614226?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	A common genetic variant is associated with adult and childhood obesity	Obesity	694 offspring	"3,489 cases, 6,392 controls, 361 trios"	NR	NR	NR		NR	NS	NS	NR	NR	"Affymetrix [86,604]"	N
11/25/2008	16252231	Maraganore	9-Sep-05	Am J Hum Genet	http://www.ncbi.nlm.nih.gov/pubmed/16252231?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	High-resolution whole-genome association study of Parkinson disease	Parkinson's disease	443 sib pairs	"332 cases, 332 controls"	5p15.2	SEMA5A	rs7702187-?	rs7702187	NR	8E-06		1.74	[1.36-2.24]	"Perlegen [198,345]"	N
11/25/2008	15761122	Klein	10-Mar-05	Science	http://www.ncbi.nlm.nih.gov/pubmed/15761122?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum	Complement factor H polymorphism in age-related macular degeneration	Age-related macular degeneration	"96 cases, 50 controls"	NR	1q31	CFH	rs380390-C	rs380390	0.70 (HapMap CEU)	4.00E-08		4.6	[2.0-11]	"Affymetrix [103,611]"	N
